Colon Cancer: Gene >> GPNMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23260117:23260117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679A>G
AA Mutation	p.Lys227Glu(p.K227E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23267939:23267939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207C>T
AA Mutation	p.Pro403Ser(p.P403S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23267889:23267889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>T
AA Mutation	p.Gly386Val(p.G386V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23254274:23254274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329C>T
AA Mutation	p.Ala110Val(p.A110V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23254184:23254184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145407985
CDS Mutation	c.239C>T
AA Mutation	p.Ala80Val(p.A80V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23253369:23253369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133A>C
AA Mutation	p.Asn45His(p.N45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23246891:23246891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34C>T
AA Mutation	p.Leu12Phe(p.L12F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23260092:23260092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.654G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23266587:23266587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23274167:23274167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745413407
CDS Mutation	c.1662G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23267971:23267971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140819013
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23246878:23246878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23270120:23270120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381990
Start	23266607:23266608(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1147dupA
AA Mutation	p.Ile383AsnfsTer9(p.I383Nfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GPNMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381990
Start	23256969:23256969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776093177
CDS Mutation	c.445G>A
AA Mutation	p.Gly149Ser(p.G149S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23260577:23260577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23267974:23267974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1242G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381990
Start	23260107:23260107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763628675
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript