Colon Cancer: Gene >> DCBLD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98819284:98819284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005A>C
AA Mutation	p.Lys335Asn(p.K335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98811301:98811301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763518499
CDS Mutation	c.1469C>T
AA Mutation	p.Thr490Met(p.T490M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98819399:98819399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890G>A
AA Mutation	p.Gly297Glu(p.G297E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98799488:98799488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212G>A
AA Mutation	p.Gly738Arg(p.G738R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98811473:98811473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143662022
CDS Mutation	c.1445C>T
AA Mutation	p.Ala482Val(p.A482V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98799461:98799461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576188055
CDS Mutation	c.2239G>A
AA Mutation	p.Glu747Lys(p.E747K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98822280:98822280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778A>G
AA Mutation	p.Lys260Glu(p.K260E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98799545:98799545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2155C>A
AA Mutation	p.Leu719Ile(p.L719I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98819212:98819212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769625584
CDS Mutation	c.1077G>T
AA Mutation	p.Lys359Asn(p.K359N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326840
Start	98812390:98812390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326840
Start	98799450:98799450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2250C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326840
Start	98819377:98819377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000326840
Start	98799421:98799421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2279C>G
AA Mutation	p.Ser760Ter(p.S760*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326840
Start	98811543:98811544(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1374_1375insTTAACAT
AA Mutation	p.Lys459LeufsTer3(p.K459Lfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000326840
Start	98825367:98825367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DCBLD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326840
Start	98881578:98881578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395G>T
AA Mutation	p.Arg132Ile(p.R132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326840
Start	98801638:98801639(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1681dupA
AA Mutation	p.Thr561AsnfsTer2(p.T561Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript