| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 8208 |
Name | CHAF1B |
Synonymous | chromatin assembly factor 1, subunit B (p60);CHAF1B;chromatin assembly factor 1, subunit B (p60) |
Definition | CAF-1 subunit B|CAF-I 60 kDa subunit|CAF-I p60|M-phase phosphoprotein 7|chromatin assembly factor 1 subunit B|chromatin assembly factor I p60 subunit|human chromatin assembly factor-I p60 subunit |
Position | 21q22.13 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1564C>T; p.P522S; 21:36415365-36415365 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.994A>G; p.T332A; 21:36411537-36411537 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1344C>T; p.D448D; 21:36413166-36413166 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1255A>C; p.T419P; 21:36413077-36413077 |
breast | carcinoma | Substitution - Missense |
c.1295C>T; p.T432M; 21:36413117-36413117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1255A>C; p.T419P; 21:36413077-36413077 |
breast | carcinoma | Substitution - Missense |
c.722G>C; p.S241T; 21:36402816-36402816 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.54C>T; p.S18S; 21:36386190-36386190 |
thyroid | other; neoplasm | Substitution - coding silent |
c.112G>A; p.D38N; 21:36386248-36386248 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1048A>T; p.S350C; 21:36411591-36411591 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.629C>T; p.S210L; 21:36399571-36399571 |
skin | malignant_melanoma | Substitution - Missense |
c.1256C>T; p.T419I; 21:36413078-36413078 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1256C>T; p.T419I; 21:36413078-36413078 |
skin | malignant_melanoma | Substitution - Missense |
c.1562C>A; p.T521N; 21:36415363-36415363 |
liver | carcinoma | Substitution - Missense |
c.270C>A; p.I90I; 21:36391561-36391561 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.720G>T; p.L240L; 21:36402814-36402814 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.112G>T; p.D38Y; 21:36386248-36386248 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.874C>T; p.R292C; 21:36409420-36409420 |
skin | malignant_melanoma | Substitution - Missense |
c.874C>T; p.R292C; 21:36409420-36409420 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.874C>T; p.R292C; 21:36409420-36409420 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1184C>A; p.P395H; 21:36413006-36413006 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1463C>G; p.T488R; 21:36413285-36413285 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1405C>G; p.L469V; 21:36413227-36413227 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1345C>T; p.P449S; 21:36413167-36413167 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.437C>T; p.S146F; 21:36394606-36394606 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.827G>A; p.R276K; 21:36408830-36408830 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.437C>T; p.S146F; 21:36394606-36394606 |
pancreas | carcinoma | Substitution - Missense |
c.688G>A; p.D230N; 21:36402782-36402782 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.489G>T; p.K163N; 21:36397422-36397422 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.471T>G; p.D157E; 21:36394640-36394640 |
skin | malignant_melanoma | Substitution - Missense |
c.1615C>T; p.P539S; 21:36416301-36416301 |
ovary | other; neoplasm | Substitution - Missense |
c.284T>G; p.V95G; 21:36391575-36391575 |
breast | carcinoma | Substitution - Missense |
c.673T>G; p.Y225D; 21:36402767-36402767 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.786A>C; p.V262V; 21:36408789-36408789 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.652G>A; p.A218T; 21:36399594-36399594 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.282G>T; p.K94N; 21:36391573-36391573 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1618C>T; p.P540S; 21:36416304-36416304 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1079T>G; p.F360C; 21:36412901-36412901 |
skin | malignant_melanoma | Substitution - Missense |
c.1462A>G; p.T488A; 21:36413284-36413284 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.219T>C; p.R73R; 21:36387690-36387690 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.571T>G; p.C191G; 21:36397504-36397504 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.587G>T; p.R196L; 21:36399529-36399529 |
skin | malignant_melanoma | Substitution - Missense |
c.98C>T; p.A33V; 21:36386234-36386234 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.396G>A; p.V132V; 21:36394565-36394565 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1607A>G; p.Q536R; 21:36416293-36416293 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.39G>T; p.K13N; 21:36386175-36386175 |
bone; rib | chondrosarcoma | Substitution - Missense |
c.591A>G; p.V197V; 21:36399533-36399533 |
breast | carcinoma | Substitution - coding silent |
c.1101C>T; p.D367D; 21:36412923-36412923 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.302C>T; p.P101L; 21:36391593-36391593 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.127-1G>T; p.?; 21:36387597-36387597 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.708C>T; p.F236F; 21:36402802-36402802 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.827+2T>C; p.?; 21:36408832-36408832 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.1148C>A; p.P383H; 21:36412970-36412970 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1152G>A; p.L384L; 21:36412974-36412974 |
skin | malignant_melanoma | Substitution - coding silent |
c.191G>A; p.R64H; 21:36387662-36387662 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.191G>A; p.R64H; 21:36387662-36387662 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.712C>T; p.R238C; 21:36402806-36402806 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1616C>T; p.P539L; 21:36416302-36416302 |
skin | malignant_melanoma | Substitution - Missense |
c.1376C>T; p.P459L; 21:36413198-36413198 |
skin | malignant_melanoma | Substitution - Missense |
c.1376C>T; p.P459L; 21:36413198-36413198 |
skin | malignant_melanoma | Substitution - Missense |
c.1376C>T; p.P459L; 21:36413198-36413198 |
skin | malignant_melanoma | Substitution - Missense |
c.835G>A; p.A279T; 21:36409381-36409381 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.922G>A; p.V308M; 21:36411465-36411465 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1540G>T; p.V514L; 21:36415341-36415341 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.721A>G; p.S241G; 21:36402815-36402815 |
liver | carcinoma | Substitution - Missense |
c.726C>T; p.F242F; 21:36402820-36402820 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.73A>G; p.T25A; 21:36386209-36386209 |
bone; pelvis | chondrosarcoma | Substitution - Missense |
c.1592C>T; p.T531M; 21:36416278-36416278 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.685C>T; p.H229Y; 21:36402779-36402779 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1391C>T; p.S464L; 21:36413213-36413213 |
prostate | carcinoma | Substitution - Missense |
c.1452C>T; p.V484V; 21:36413274-36413274 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.1452C>T; p.V484V; 21:36413274-36413274 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1375C>T; p.P459S; 21:36413197-36413197 |
skin | malignant_melanoma | Substitution - Missense |
c.695G>A; p.S232N; 21:36402789-36402789 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.190C>T; p.R64C; 21:36387661-36387661 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1630C>T; p.R544W; 21:36416316-36416316 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |