Primary Site >> Stomach Cancer

Gene >> WWC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183261008:183261008(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758105845
CDS Mutation c.1385A>G
AA Mutation p.Asn462Ser(p.N462S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183261323:183261323(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766503307
CDS Mutation c.1700C>T
AA Mutation p.Thr567Met(p.T567M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183245484:183245484(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.671A>C
AA Mutation p.Glu224Ala(p.E224A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183261046:183261046(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757318662
CDS Mutation c.1423A>C
AA Mutation p.Ser475Arg(p.S475R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183253920:183253920(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755775249
CDS Mutation c.1117C>T
AA Mutation p.Arg373Cys(p.R373C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183253902:183253902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1099A>G
AA Mutation p.Thr367Ala(p.T367A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000403733
Start 183312385:183312385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3429G>C
AA Mutation p.Glu1143Asp(p.E1143D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000403733
Start 183261276:183261276(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1653C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000403733
Start 183284297:183284297(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2955C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000403733
Start 183245423:183245423(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.616delA
AA Mutation p.Met206CysfsTer17(p.M206Cfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000403733
Start 183265946:183265946(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2205delA
AA Mutation p.Val736TyrfsTer49(p.V736Yfs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript