Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HM13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340852
Start	31554797:31554797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>T
AA Mutation	p.Ala259Val(p.A259V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340852
Start	31569191:31569191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106C>T
AA Mutation	p.Ser369Leu(p.S369L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340852
Start	31566263:31566263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567853849
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340852
Start	31538226:31538226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753154758
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340852
Start	31549063:31549063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489G>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HM13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340852
Start	31569182:31569182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097C>T
AA Mutation	p.Ala366Val(p.A366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340852
Start	31527496:31527496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196A>C
AA Mutation	p.Met66Leu(p.M66L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340852
Start	31527497:31527497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197T>A
AA Mutation	p.Met66Lys(p.M66K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340852
Start	31550103:31550103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706T>C
AA Mutation	p.Phe236Leu(p.F236L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript