Colon Cancer: Gene >> CD248

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315750:66315750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1278G>T
AA Mutation	p.Glu426Asp(p.E426D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66314894:66314894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747726735
CDS Mutation	c.2134C>T
AA Mutation	p.Arg712Cys(p.R712C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66314849:66314849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2179C>T
AA Mutation	p.Arg727Cys(p.R727C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315002:66315002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773387758
CDS Mutation	c.2026C>T
AA Mutation	p.Leu676Phe(p.L676F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315661:66315661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539641105
CDS Mutation	c.1367C>T
AA Mutation	p.Thr456Met(p.T456M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315595:66315595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202170042
CDS Mutation	c.1433G>A
AA Mutation	p.Arg478His(p.R478H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315319:66315319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1709C>A
AA Mutation	p.Pro570Gln(p.P570Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315419:66315419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140856103
CDS Mutation	c.1609C>T
AA Mutation	p.Arg537Trp(p.R537W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316354:66316354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565157270
CDS Mutation	c.674G>A
AA Mutation	p.Arg225Gln(p.R225Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66314996:66314996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373617917
CDS Mutation	c.2032G>A
AA Mutation	p.Glu678Lys(p.E678K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316636:66316636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392G>A
AA Mutation	p.Cys131Tyr(p.C131Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66315825:66315825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113882023
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66315252:66315252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66314961:66314961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2067G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66316215:66316215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761673984
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311330
Start	66314799:66314799(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2229delC
AA Mutation	p.Arg744GlyfsTer61(p.R744Gfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311330
Start	66315011:66315011(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2017delG
AA Mutation	p.Glu673ArgfsTer132(p.E673Rfs*132)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311330
Start	66315010:66315011(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2017dupG
AA Mutation	p.Glu673GlyfsTer12(p.E673Gfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD248

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66315819:66315819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186642249
CDS Mutation	c.1209G>A
Mutation Classification	Silent
Feature Type	Transcript