Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SPDYA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000334056
Start 28849925:28849925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753354043
CDS Mutation c.926C>T
AA Mutation p.Thr309Ile(p.T309I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000334056
Start 28822392:28822392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.362T>C
AA Mutation p.Ile121Thr(p.I121T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000334056
Start 28829194:28829194(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771698422
CDS Mutation c.427G>A
AA Mutation p.Glu143Lys(p.E143K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000334056
Start 28840178:28840178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.559G>A
AA Mutation p.Ala187Thr(p.A187T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000334056
Start 28829254:28829254(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.487T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000334056
Start 28840361:28840361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775407305
CDS Mutation c.742T>C
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> SPDYA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000334056
Start 28816102:28816102(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.88A>C
AA Mutation p.Lys30Gln(p.K30Q)
Mutation Classification Missense_Mutation
Feature Type Transcript