Primary Site >> Stomach Cancer

Gene >> PRPF6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63983084:63983084(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.109G>A
AA Mutation p.Ala37Thr(p.A37T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64032925:64032925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766740751
CDS Mutation c.2758G>A
AA Mutation p.Ala920Thr(p.A920T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64031935:64031935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2564G>A
AA Mutation p.Arg855Gln(p.R855Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63993428:63993428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.381A>C
AA Mutation p.Glu127Asp(p.E127D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64010244:64010244(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771579599
CDS Mutation c.1231G>A
AA Mutation p.Val411Ile(p.V411I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64026009:64026009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1979G>A
AA Mutation p.Arg660Gln(p.R660Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 63999743:63999743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1007C>T
AA Mutation p.Thr336Met(p.T336M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64027144:64027144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2191G>A
AA Mutation p.Ala731Thr(p.A731T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000266079
Start 64022851:64022851(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1742C>T
AA Mutation p.Ala581Val(p.A581V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000266079
Start 64032888:64032888(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2721G>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000266079
Start 63983182:63983182(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.207C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000266079
Start 63999630:63999630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.894C>G
Mutation Classification Silent
Feature Type Transcript