Colon Cancer: Gene >> ANPEP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89792254:89792254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759355791
CDS Mutation	c.2434G>A
AA Mutation	p.Ala812Thr(p.A812T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89804575:89804575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148047449
CDS Mutation	c.940G>A
AA Mutation	p.Gly314Ser(p.G314S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89785474:89785474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2779G>A
AA Mutation	p.Glu927Lys(p.E927K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89797634:89797634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2098A>C
AA Mutation	p.Ser700Arg(p.S700R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89806280:89806280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769850318
CDS Mutation	c.304G>A
AA Mutation	p.Val102Ile(p.V102I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89806001:89806001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201704361
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Cys(p.R195C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89806084:89806084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>G
AA Mutation	p.Lys167Arg(p.K167R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89793077:89793077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2207A>C
AA Mutation	p.Asn736Thr(p.N736T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89799297:89799297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972C>T
AA Mutation	p.Arg658Trp(p.R658W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89791059:89791059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369201239
CDS Mutation	c.2563C>T
AA Mutation	p.Arg855Trp(p.R855W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89799294:89799294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1975G>A
AA Mutation	p.Ala659Thr(p.A659T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89803747:89803747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337T>C
AA Mutation	p.Val446Ala(p.V446A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89797718:89797718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014C>T
AA Mutation	p.His672Tyr(p.H672Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89803253:89803253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>A
AA Mutation	p.Asp519Asn(p.D519N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89806407:89806407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781513331
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89806038:89806038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779724705
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89792285:89792285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2403C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89804349:89804349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89792321:89792321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2367C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89803722:89803722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747845929
CDS Mutation	c.1362G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89803907:89803907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369610508
CDS Mutation	c.1275G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300060
Start	89803710:89803710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779974811
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000300060
Start	89806241:89806241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>T
AA Mutation	p.Glu115Ter(p.E115*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANPEP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300060
Start	89799473:89799473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774559825
CDS Mutation	c.1906G>A
AA Mutation	p.Glu636Lys(p.E636K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript