Colon Cancer: Gene >> VWA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114255025:114255025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562799356
CDS Mutation	c.238G>A
AA Mutation	p.Gly80Ser(p.G80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114278038:114278038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200329465
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114285999:114285999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058G>A
AA Mutation	p.Gly353Asp(p.G353D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114286334:114286334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393G>T
AA Mutation	p.Ala465Ser(p.A465S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114290333:114290333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761365199
CDS Mutation	c.2216G>A
AA Mutation	p.Arg739Gln(p.R739Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114289364:114289364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1997G>T
AA Mutation	p.Gly666Val(p.G666V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114272898:114272898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530G>A
AA Mutation	p.Gly177Asp(p.G177D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114286335:114286335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768986747
CDS Mutation	c.1394C>T
AA Mutation	p.Ala465Val(p.A465V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114286076:114286076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768024904
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Trp(p.R379W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114286313:114286313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560050132
CDS Mutation	c.1372G>A
AA Mutation	p.Glu458Lys(p.E458K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114272837:114272837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569122106
CDS Mutation	c.469G>A
AA Mutation	p.Val157Ile(p.V157I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114290307:114290307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2190G>T
AA Mutation	p.Gln730His(p.Q730H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114286326:114286326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200547974
CDS Mutation	c.1385C>T
AA Mutation	p.Ala462Val(p.A462V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392982
Start	114278028:114278028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392982
Start	114289365:114289365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771998666
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392982
Start	114272752:114272752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761067619
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392982
Start	114289440:114289440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148020287
CDS Mutation	c.2073C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392982
Start	114286012:114286012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775011963
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392982
Start	114255024:114255024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748070852
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VWA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114285951:114285951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010G>T
AA Mutation	p.Ser337Ile(p.S337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392982
Start	114289237:114289237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376331052
CDS Mutation	c.1870G>A
AA Mutation	p.Val624Ile(p.V624I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript