Colon Cancer: Gene >> BAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52405800:52405800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896A>G
AA Mutation	p.Asn299Ser(p.N299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52403208:52403208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770654975
CDS Mutation	c.1820C>T
AA Mutation	p.Thr607Met(p.T607M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52403709:52403709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436C>T
AA Mutation	p.Pro479Leu(p.P479L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52405214:52405214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012C>T
AA Mutation	p.Pro338Ser(p.P338S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52406869:52406869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Trp(p.R207W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52402326:52402326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2152C>T
AA Mutation	p.Arg718Trp(p.R718W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460680
Start	52408570:52408570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187643606
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460680
Start	52402645:52402645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200194082
CDS Mutation	c.2013C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460680
Start	52403219:52403219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1809C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460680
Start	52407196:52407196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460680
Start	52403807:52403807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763735807
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000460680
Start	52405882:52405882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>T
AA Mutation	p.Gln272Ter(p.Q272*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52402329:52402329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2149C>T
AA Mutation	p.Arg717Trp(p.R717W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000460680
Start	52403623:52403623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522C>T
AA Mutation	p.Arg508Cys(p.R508C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript