Colon Cancer: Gene >> CHPF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151237624:151237624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746382000
CDS Mutation	c.1262G>A
AA Mutation	p.Arg421His(p.R421H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151235248:151235248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752470752
CDS Mutation	c.464G>A
AA Mutation	p.Arg155Gln(p.R155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151238415:151238415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146697508
CDS Mutation	c.2053C>T
AA Mutation	p.Arg685Trp(p.R685W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151238158:151238158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1796C>A
AA Mutation	p.Pro599His(p.P599H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151235497:151235497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116843667
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151237383:151237383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766740377
CDS Mutation	c.1021C>T
AA Mutation	p.Arg341Trp(p.R341W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000035307
Start	151238055:151238055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374488900
CDS Mutation	c.1693G>A
AA Mutation	p.Ala565Thr(p.A565T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000035307
Start	151238096:151238096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567259830
CDS Mutation	c.1734C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000035307
Start	151234038:151234038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000035307
Start	151235303:151235303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139063090
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000035307
Start	151238144:151238144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766686871
CDS Mutation	c.1782C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000035307
Start	151237517:151237517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000035307
Start	151237898:151237899(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1538dupA
AA Mutation	p.Asn513LysfsTer133(p.N513Kfs*133)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000035307
Start	151237514:151237516(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1154_1156delCCT
AA Mutation	p.Ser385del(p.S385del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000035307
Start	151237511:151237513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1151_1153delTCT
AA Mutation	p.Phe384del(p.F384del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CHPF2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000035307
Start	151237814:151237814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452T>C
Mutation Classification	Silent
Feature Type	Transcript