Colon Cancer: Gene >> GPD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156550607:156550607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746974136
CDS Mutation	c.832G>A
AA Mutation	p.Glu278Lys(p.E278K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156510825:156510825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304G>T
AA Mutation	p.Asp102Tyr(p.D102Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310454
Start	156570218:156570218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608G>T
AA Mutation	p.Glu536Asp(p.E536D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156568912:156568912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373946105
CDS Mutation	c.1253G>A
AA Mutation	p.Arg418Gln(p.R418Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156578938:156578938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817A>C
AA Mutation	p.Lys606Thr(p.K606T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156510820:156510820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>T
AA Mutation	p.Arg100Ile(p.R100I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156582899:156582899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2165G>A
AA Mutation	p.Arg722His(p.R722H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156569384:156569384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140203221
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441Gln(p.R441Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310454
Start	156476135:156476135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572409828
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310454
Start	156569535:156569535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201926174
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310454
Start	156513444:156513444(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.611delT
AA Mutation	p.Phe204SerfsTer10(p.F204Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156510832:156510832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>T
AA Mutation	p.Ser104Leu(p.S104L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156579132:156579132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1927A>C
AA Mutation	p.Ile643Leu(p.I643L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310454
Start	156569407:156569407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345A>C
AA Mutation	p.Asn449His(p.N449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript