Colon Cancer: Gene >> CHFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132861554:132861554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35206714
CDS Mutation	c.700C>T
AA Mutation	p.Leu234Phe(p.L234F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132851630:132851630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746554223
CDS Mutation	c.1516G>A
AA Mutation	p.Ala506Thr(p.A506T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000432561
Start	132847043:132847043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771G>T
AA Mutation	p.Asp591Tyr(p.D591Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132861536:132861536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533118486
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132856547:132856547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Trp(p.R396W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132856543:132856543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190C>A
AA Mutation	p.Ser397Tyr(p.S397Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132872375:132872375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253A>G
AA Mutation	p.Asn85Asp(p.N85D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432561
Start	132843049:132843049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1914C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432561
Start	132848094:132848094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1674C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432561
Start	132853492:132853492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374006779
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432561
Start	132857547:132857547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000432561
Start	132872338:132872339(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.289_290delTT
AA Mutation	p.Leu97ThrfsTer14(p.L97Tfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CHFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132861526:132861526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754307363
CDS Mutation	c.728C>T
AA Mutation	p.Ser243Leu(p.S243L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432561
Start	132872317:132872317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311A>G
AA Mutation	p.Tyr104Cys(p.Y104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000432561
Start	132847131:132847131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1684-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript