Primary Site >> Stomach Cancer

Gene >> COL4A6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108170629:108170629(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3476C>T
AA Mutation p.Pro1159Leu(p.P1159L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108163035:108163035(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4076C>G
AA Mutation p.Ser1359Cys(p.S1359C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108214201:108214201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.355G>T
AA Mutation p.Gly119Cys(p.G119C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108159559:108159559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4718C>T
AA Mutation p.Ala1573Val(p.A1573V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108162936:108162936(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4175G>A
AA Mutation p.Gly1392Asp(p.G1392D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108170702:108170702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3403G>T
AA Mutation p.Ala1135Ser(p.A1135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108160628:108160628(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4363G>A
AA Mutation p.Gly1455Arg(p.G1455R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108165024:108165024(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113329155
CDS Mutation c.3826G>A
AA Mutation p.Ala1276Thr(p.A1276T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000372216
Start 108179354:108179354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2219G>A
AA Mutation p.Ser740Asn(p.S740N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000372216
Start 108175733:108175733(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2754A>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000372216
Start 108174446:108174446(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3135A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000372216
Start 108169562:108169562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3627A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000372216
Start 108187268:108187268(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1782A>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000372216
Start 108180608:108180608(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2041C>T
AA Mutation p.Arg681Ter(p.R681*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence splice_donor_variant
Transcription ID ENST00000372216
Start 108205437:108205437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.690+2T>C
Mutation Classification Splice_Site
Feature Type Transcript