Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NFKB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102529902:102529902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.106G>A
AA Mutation p.Ala36Thr(p.A36T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102606583:102606583(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374903458
CDS Mutation c.1837C>T
AA Mutation p.Arg613Cys(p.R613C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102612530:102612530(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2513A>G
AA Mutation p.Lys838Arg(p.K838R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102606611:102606611(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1865C>T
AA Mutation p.Ala622Val(p.A622V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102584696:102584696(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.939C>A
AA Mutation p.Phe313Leu(p.F313L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102597585:102597585(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767590342
CDS Mutation c.1558G>A
AA Mutation p.Ala520Thr(p.A520T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102584715:102584715(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.958G>T
AA Mutation p.Asp320Tyr(p.D320Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102600927:102600927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1667C>T
AA Mutation p.Ser556Phe(p.S556F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102578950:102578950(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.638G>A
AA Mutation p.Arg213Gln(p.R213Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000394820
Start 102607672:102607672(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2145T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000394820
Start 102613497:102613497(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2662delA
AA Mutation p.Ile888SerfsTer8(p.I888Sfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> NFKB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102606584:102606584(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773613546
CDS Mutation c.1838G>A
AA Mutation p.Arg613His(p.R613H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102577034:102577034(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.563T>G
AA Mutation p.Leu188Arg(p.L188R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102579034:102579034(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.722A>G
AA Mutation p.Asp241Gly(p.D241G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102537867:102537867(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.166C>T
AA Mutation p.Arg56Cys(p.R56C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102593473:102593473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371719137
CDS Mutation c.1112C>T
AA Mutation p.Ser371Leu(p.S371L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102613543:102613543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142074302
CDS Mutation c.2708C>T
AA Mutation p.Ser903Leu(p.S903L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000394820
Start 102594895:102594895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1211A>C
AA Mutation p.Tyr404Ser(p.Y404S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000394820
Start 102597599:102597599(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1572C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000394820
Start 102596311:102596311(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1471G>T
AA Mutation p.Glu491Ter(p.E491*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript