Colon Cancer: Gene >> CHTF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	792335:792335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314C>A
AA Mutation	p.Asp438Glu(p.D438E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	794122:794122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774472730
CDS Mutation	c.1871C>T
AA Mutation	p.Ser624Phe(p.S624F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	793165:793165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200233056
CDS Mutation	c.1693C>T
AA Mutation	p.Arg565Trp(p.R565W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	794076:794076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377736001
CDS Mutation	c.1825G>A
AA Mutation	p.Ala609Thr(p.A609T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	791918:791918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373070511
CDS Mutation	c.1172C>T
AA Mutation	p.Ala391Val(p.A391V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	797845:797845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2294453
CDS Mutation	c.2798C>T
AA Mutation	p.Thr933Met(p.T933M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	797946:797946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372760513
CDS Mutation	c.2899C>T
AA Mutation	p.Arg967Cys(p.R967C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	789665:789665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374092978
CDS Mutation	c.556G>A
AA Mutation	p.Val186Ile(p.V186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	789338:789338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415C>A
AA Mutation	p.Leu139Ile(p.L139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	789687:789687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768976698
CDS Mutation	c.578G>A
AA Mutation	p.Arg193His(p.R193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	794133:794133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760424990
CDS Mutation	c.1882G>A
AA Mutation	p.Ala628Thr(p.A628T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	797875:797875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373749220
CDS Mutation	c.2828G>A
AA Mutation	p.Arg943His(p.R943H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	791902:791902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156G>A
AA Mutation	p.Val386Met(p.V386M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262315
Start	797726:797726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2766C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262315
Start	791901:791901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201986546
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262315
Start	792546:792546(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1440delG
AA Mutation	p.Leu481SerfsTer3(p.L481Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CHTF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	797845:797845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2294453
CDS Mutation	c.2798C>T
AA Mutation	p.Thr933Met(p.T933M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262315
Start	797875:797875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373749220
CDS Mutation	c.2828G>A
AA Mutation	p.Arg943His(p.R943H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262315
Start	789322:789322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368449098
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript