Primary Site >> Stomach Cancer

Gene >> CRYGD

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264376
Start 208124144:208124144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.220G>A
AA Mutation p.Asp74Asn(p.D74N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264376
Start 208124171:208124171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.193G>A
AA Mutation p.Asp65Asn(p.D65N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000264376
Start 208124187:208124187(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.177C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000264376
Start 208121723:208121723(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.475delG
AA Mutation p.Ala159ProfsTer9(p.A159Pfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000264376
Start 208121721:208121721(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.477delC
AA Mutation p.Thr160ArgfsTer8(p.T160Rfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript