Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HDC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50254619:50254619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.487A>C
AA Mutation p.Lys163Gln(p.K163Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50254162:50254162(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.688G>A
AA Mutation p.Glu230Lys(p.E230K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50254637:50254637(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.469G>T
AA Mutation p.Ala157Ser(p.A157S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50242501:50242501(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777905414
CDS Mutation c.1748G>A
AA Mutation p.Arg583His(p.R583H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50242957:50242957(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1292G>A
AA Mutation p.Gly431Asp(p.G431D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50242424:50242424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1825T>G
AA Mutation p.Ser609Ala(p.S609A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000267845
Start 50254178:50254178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.672T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000267845
Start 50242983:50242983(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1266T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000267845
Start 50263238:50263238(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776800647
CDS Mutation c.201T>C
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> HDC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50242434:50242434(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1815G>C
AA Mutation p.Lys605Asn(p.K605N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50254660:50254660(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751827833
CDS Mutation c.446C>T
AA Mutation p.Thr149Met(p.T149M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50263318:50263318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.121G>A
AA Mutation p.Ala41Thr(p.A41T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50242380:50242380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1869G>T
AA Mutation p.Met623Ile(p.M623I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50242541:50242541(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1708T>C
AA Mutation p.Phe570Leu(p.F570L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50258447:50258447(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.275G>T
AA Mutation p.Gly92Val(p.G92V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000267845
Start 50254223:50254223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.627A>T
AA Mutation p.Lys209Asn(p.K209N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000267845
Start 50263236:50263236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.203G>A
AA Mutation p.Gly68Glu(p.G68E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000267845
Start 50252463:50252463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1008G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000267845
Start 50243220:50243220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1165G>T
AA Mutation p.Glu389Ter(p.E389*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000267845
Start 50263321:50263321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750405599
CDS Mutation c.118C>T
AA Mutation p.Arg40Ter(p.R40*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000267845
Start 50242847:50242847(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756593325
CDS Mutation c.1402C>T
AA Mutation p.Arg468Ter(p.R468*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript