Colon Cancer: Gene >> KLRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336164
Start	10311514:10311514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214T>C
AA Mutation	p.Cys72Arg(p.C72R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336164
Start	10309457:10309457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201683513
CDS Mutation	c.77C>T
AA Mutation	p.Thr26Met(p.T26M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336164
Start	10311477:10311477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336164
Start	10311487:10311488(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.192dupA
AA Mutation	p.Trp65MetfsTer14(p.W65Mfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336164
Start	10311537:10311538(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.241dupA
AA Mutation	p.Thr81AsnfsTer24(p.T81Nfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KLRD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336164
Start	10309445:10309445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755827000
CDS Mutation	c.65C>T
AA Mutation	p.Ser22Leu(p.S22L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript