Colon Cancer: Gene >> ENPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131869418:131869418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771292916
CDS Mutation	c.1334A>C
AA Mutation	p.Lys445Thr(p.K445T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131861608:131861608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Ala310Val(p.A310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131882352:131882352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2108T>C
AA Mutation	p.Phe703Ser(p.F703S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131883728:131883728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2265A>C
AA Mutation	p.Glu755Asp(p.E755D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131886660:131886660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2543G>A
AA Mutation	p.Cys848Tyr(p.C848Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131890467:131890467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2734T>G
AA Mutation	p.Leu912Val(p.L912V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131890444:131890444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2711G>T
AA Mutation	p.Arg904Ile(p.R904I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131858704:131858704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752T>C
AA Mutation	p.Val251Ala(p.V251A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131874330:131874330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628A>T
AA Mutation	p.Asn543Ile(p.N543I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131877024:131877024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756G>A
AA Mutation	p.Gly586Arg(p.G586R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360971
Start	131847790:131847790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360971
Start	131879890:131879890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1956T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360971
Start	131873012:131873012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1527C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360971
Start	131884998:131884998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755592935
CDS Mutation	c.2379C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360971
Start	131858688:131858688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759257042
CDS Mutation	c.740delA
AA Mutation	p.Asn247ThrfsTer2(p.N247Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000360971
Start	131872069:131872069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1406-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000360971
Start	131874328:131874329(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1626_1627insTTG
AA Mutation	p.Ser542_Asn543insLeu(p.S542_N543insL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ENPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360971
Start	131879886:131879886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1952T>G
AA Mutation	p.Ile651Ser(p.I651S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360971
Start	131886718:131886718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2601C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000360971
Start	131878541:131878541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1894-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript