Colon Cancer: Gene >> SFRP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274063
Start	153781473:153781473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866G>A
AA Mutation	p.Ser289Asn(p.S289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274063
Start	153781468:153781468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774857018
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Cys(p.R291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274063
Start	153781576:153781576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778665160
CDS Mutation	c.763G>A
AA Mutation	p.Ala255Thr(p.A255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274063
Start	153788488:153788488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760558817
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274063
Start	153781586:153781586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274063
Start	153788650:153788650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779169377
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274063
Start	153788431:153788431(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.405delC
AA Mutation	p.Trp136GlyfsTer50(p.W136Gfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000274063
Start	153788670:153788670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>T
AA Mutation	p.Gln56Ter(p.Q56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SFRP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274063
Start	153788737:153788737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>A
AA Mutation	p.Phe33Leu(p.F33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274063
Start	153781634:153781634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143701440
CDS Mutation	c.705G>A
Mutation Classification	Silent
Feature Type	Transcript