Colon Cancer: Gene >> CTCFL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57518819:57518819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998G>A
AA Mutation	p.Arg333His(p.R333H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000243914
Start	57519375:57519375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774266834
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57518820:57518820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Cys(p.R333C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57514655:57514655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765675257
CDS Mutation	c.1267G>A
AA Mutation	p.Glu423Lys(p.E423K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57512675:57512675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1408C>T
AA Mutation	p.Arg470Cys(p.R470C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57524028:57524028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>A
AA Mutation	p.Val60Ile(p.V60I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57512720:57512720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572666290
CDS Mutation	c.1363G>A
AA Mutation	p.Ala455Thr(p.A455T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57519370:57519370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762A>C
AA Mutation	p.Lys254Asn(p.K254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57518856:57518856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961G>A
AA Mutation	p.Ala321Thr(p.A321T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243914
Start	57515805:57515805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1089C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243914
Start	57498614:57498617(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1925_1928delCCAG
AA Mutation	p.Ala642GlufsTer10(p.A642Efs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243914
Start	57524131:57524131(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.75delA
AA Mutation	p.Gly26AlafsTer2(p.G26Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTCFL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57524187:57524187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19T>A
AA Mutation	p.Ser7Thr(p.S7T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243914
Start	57523238:57523238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584G>T
AA Mutation	p.Arg195Ile(p.R195I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243914
Start	57523103:57523103(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.719delA
AA Mutation	p.Lys240ArgfsTer37(p.K240Rfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript