Primary Site >> Stomach Cancer

Gene >> ATP2A2

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000539276
Start 110327554:110327554(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.632G>A
AA Mutation p.Gly211Asp(p.G211D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000539276
Start 110332661:110332661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1160C>T
AA Mutation p.Ser387Leu(p.S387L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000539276
Start 110342315:110342315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2185G>A
AA Mutation p.Ala729Thr(p.A729T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000539276
Start 110339573:110339573(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1613C>A
AA Mutation p.Ser538Tyr(p.S538Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000539276
Start 110345334:110345334(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2693T>C
AA Mutation p.Met898Thr(p.M898T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000539276
Start 110343375:110343375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778998667
CDS Mutation c.2462G>A
AA Mutation p.Arg821Gln(p.R821Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000539276
Start 110296607:110296607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.333T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000539276
Start 110340739:110340739(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1842G>A
Mutation Classification Silent
Feature Type Transcript