Colon Cancer: Gene >> TFDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113631723:113631723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287A>C
AA Mutation	p.Asp96Ala(p.D96A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113633942:113633942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527T>A
AA Mutation	p.Leu176Gln(p.L176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113611026:113611026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43A>C
AA Mutation	p.Lys15Gln(p.K15Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000375370
Start	113634601:113634601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>G
AA Mutation	p.Gln229Arg(p.Q229R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113634014:113634014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>T
AA Mutation	p.Gln200Leu(p.Q200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113623209:113623209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109T>A
AA Mutation	p.Ser37Thr(p.S37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113633918:113633918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113636106:113636106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>A
AA Mutation	p.Asp273Asn(p.D273N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113611011:113611011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28G>A
AA Mutation	p.Ala10Thr(p.A10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375370
Start	113631652:113631652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149994612
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375370
Start	113633231:113633231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375370
Start	113636558:113636558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763022738
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000375370
Start	113633969:113633971(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.559_561delAAG
AA Mutation	p.Lys187del(p.K187del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TFDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113631722:113631722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773698836
CDS Mutation	c.286G>A
AA Mutation	p.Asp96Asn(p.D96N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375370
Start	113636582:113636582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>A
AA Mutation	p.Asp296Glu(p.D296E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript