Colon Cancer: Gene >> CARD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852596:40852596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>A
AA Mutation	p.Gly422Arg(p.G422R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852708:40852708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199835164
CDS Mutation	c.1376G>A
AA Mutation	p.Arg459His(p.R459H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852305:40852305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973T>A
AA Mutation	p.Leu325Ile(p.L325I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40853844:40853844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765490996
CDS Mutation	c.2512A>G
AA Mutation	p.Thr838Ala(p.T838A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852506:40852506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183932779
CDS Mutation	c.1174C>T
AA Mutation	p.Arg392Cys(p.R392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852507:40852507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377732886
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392His(p.R392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40841600:40841600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218A>C
AA Mutation	p.Gln73Pro(p.Q73P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40853281:40853281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949C>T
AA Mutation	p.Ala650Val(p.A650V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852592:40852592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260G>T
AA Mutation	p.Met420Ile(p.M420I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40854013:40854013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2681C>A
AA Mutation	p.Pro894His(p.P894H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852762:40852762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430C>A
AA Mutation	p.Pro477His(p.P477H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40841442:40841442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60A>C
AA Mutation	p.Glu20Asp(p.E20D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852945:40852945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613G>T
AA Mutation	p.Ser538Ile(p.S538I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40841398:40841398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16A>G
AA Mutation	p.Thr6Ala(p.T6A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852707:40852707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561968147
CDS Mutation	c.1375C>T
AA Mutation	p.Arg459Cys(p.R459C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40853341:40853341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2009C>G
AA Mutation	p.Ser670Cys(p.S670C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254691
Start	40854107:40854107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2775A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254691
Start	40853388:40853388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2056A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254691
Start	40841397:40841397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767188573
CDS Mutation	c.15T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CARD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852800:40852800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468G>T
AA Mutation	p.Asp490Tyr(p.D490Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40841486:40841486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104C>T
AA Mutation	p.Ser35Phe(p.S35F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254691
Start	40852882:40852882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550G>T
AA Mutation	p.Arg517Ile(p.R517I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript