Colon Cancer: Gene >> CFAP97

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185191144:185191144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53A>G
AA Mutation	p.Asp18Gly(p.D18G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000458385
Start	185162925:185162925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1472G>A
AA Mutation	p.Arg491Lys(p.R491K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185164103:185164103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777547282
CDS Mutation	c.1397G>A
AA Mutation	p.Arg466His(p.R466H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185190422:185190422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775T>C
AA Mutation	p.Ser259Pro(p.S259P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185176037:185176037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069G>A
AA Mutation	p.Asp357Asn(p.D357N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185190702:185190702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495G>T
AA Mutation	p.Lys165Asn(p.K165N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458385
Start	185190903:185190903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458385
Start	185190858:185190858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141482103
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458385
Start	185190890:185190891(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.306dupA
AA Mutation	p.Leu103IlefsTer3(p.L103Ifs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CFAP97

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185190829:185190829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368T>G
AA Mutation	p.Ile123Ser(p.I123S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185190511:185190511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686C>T
AA Mutation	p.Ser229Leu(p.S229L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000458385
Start	185191039:185191039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373566490
CDS Mutation	c.158C>T
AA Mutation	p.Ser53Leu(p.S53L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript