Colon Cancer: Gene >> GPC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	93227536:93227536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775575495
CDS Mutation	c.80C>T
AA Mutation	p.Ala27Val(p.A27V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	94382534:94382534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273G>A
AA Mutation	p.Gly425Arg(p.G425R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	94306118:94306118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771182029
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Trp(p.R383W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	94398579:94398579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764440422
CDS Mutation	c.1403G>A
AA Mutation	p.Arg468His(p.R468H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	94403051:94403051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746531582
CDS Mutation	c.1502G>T
AA Mutation	p.Cys501Phe(p.C501F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	93830324:93830324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490T>A
AA Mutation	p.Phe164Ile(p.F164I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	93545386:93545386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>A
AA Mutation	p.Arg95His(p.R95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	94306101:94306101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130C>A
AA Mutation	p.Ala377Glu(p.A377E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	94403126:94403126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1577A>C
AA Mutation	p.Glu526Ala(p.E526A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	93830220:93830220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386G>A
AA Mutation	p.Gly129Asp(p.G129D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	94398604:94398604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146868653
CDS Mutation	c.1428C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	94382533:94382533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200389469
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	94027833:94027833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113591716
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	93227564:93227564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	93227519:93227519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	94286413:94286413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138238361
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	94286368:94286368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377047
Start	94403157:94403157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000377047
Start	93545300:93545300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198C>A
AA Mutation	p.Cys66Ter(p.C66*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377047
Start	93545386:93545386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284G>T
AA Mutation	p.Arg95Leu(p.R95L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript