Colon Cancer: Gene >> SERINC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339697
Start	122451997:122451997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650T>G
AA Mutation	p.Phe217Cys(p.F217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339697
Start	122447183:122447183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339697
Start	122456513:122456513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000339697
Start	122447266:122447266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SERINC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339697
Start	122445058:122445058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339697
Start	122451956:122451956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138235986
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339697
Start	122453856:122453856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503T>G
AA Mutation	p.Leu168Arg(p.L168R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339697
Start	122453786:122453786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751011270
CDS Mutation	c.573G>A
Mutation Classification	Silent
Feature Type	Transcript