Colon Cancer: Gene >> CD276

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73702449:73702449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562558740
CDS Mutation	c.274C>T
AA Mutation	p.Arg92Cys(p.R92C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73702488:73702488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751833994
CDS Mutation	c.313G>A
AA Mutation	p.Ala105Thr(p.A105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73702555:73702555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780694082
CDS Mutation	c.380G>A
AA Mutation	p.Arg127Gln(p.R127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73704244:73704244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769999909
CDS Mutation	c.1141A>G
AA Mutation	p.Ile381Val(p.I381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73704284:73704284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181T>C
AA Mutation	p.Val394Ala(p.V394A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73702573:73702573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>A
AA Mutation	p.Ala133Asp(p.A133D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73702308:73702308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541095307
CDS Mutation	c.133G>A
AA Mutation	p.Asp45Asn(p.D45N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318443
Start	73703917:73703917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762931731
CDS Mutation	c.992G>A
AA Mutation	p.Arg331His(p.R331H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318443
Start	73712936:73712936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585G>T
AA Mutation	p.Asp529Tyr(p.D529Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318443
Start	73711137:73711137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1549C>A
AA Mutation	p.Leu517Met(p.L517M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318443
Start	73704418:73704418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD276

No Mutation Annotation!