Colon Cancer: Gene >> REPIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397281
Start	150371552:150371552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376711625
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397281
Start	150371308:150371308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67C>T
AA Mutation	p.Pro23Ser(p.P23S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397281
Start	150372903:150372903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397281
Start	150372350:150372350(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759247453
CDS Mutation	c.1116delC
AA Mutation	p.Ser373ProfsTer242(p.S373Pfs*242)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000397281
Start	150371710:150371710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Ter(p.R157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> REPIN1

No Mutation Annotation!