Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF835

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663953:56663953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Trp(p.R416W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664517:56664517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776888606
CDS Mutation	c.682G>A
AA Mutation	p.Ala228Thr(p.A228T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663935:56663935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1264G>A
AA Mutation	p.Glu422Lys(p.E422K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664723:56664723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476C>T
AA Mutation	p.Thr159Met(p.T159M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664390:56664390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>A
AA Mutation	p.Arg270His(p.R270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664007:56664007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192G>A
AA Mutation	p.Ala398Thr(p.A398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664906:56664906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746101788
CDS Mutation	c.293G>A
AA Mutation	p.Arg98His(p.R98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664261:56664261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746857795
CDS Mutation	c.938C>T
AA Mutation	p.Ala313Val(p.A313V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663700:56663700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1499C>T
AA Mutation	p.Ser500Leu(p.S500L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663899:56663899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750603570
CDS Mutation	c.1300G>A
AA Mutation	p.Ala434Thr(p.A434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663604:56663604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595G>A
AA Mutation	p.Arg532His(p.R532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664052:56664052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>A
AA Mutation	p.Val383Met(p.V383M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663590:56663590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609G>A
AA Mutation	p.Asp537Asn(p.D537N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664093:56664093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106A>C
AA Mutation	p.Lys369Thr(p.K369T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663791:56663791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746617831
CDS Mutation	c.1408G>A
AA Mutation	p.Gly470Arg(p.G470R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56665108:56665108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91C>G
AA Mutation	p.Gln31Glu(p.Q31E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664945:56664945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664717:56664717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482C>T
AA Mutation	p.Thr161Met(p.T161M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56665023:56665023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176G>A
AA Mutation	p.Arg59Gln(p.R59Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664601:56664601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528976354
CDS Mutation	c.598G>A
AA Mutation	p.Gly200Ser(p.G200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663736:56663736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1463C>T
AA Mutation	p.Ala488Val(p.A488V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664726:56664726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663737:56663737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462G>A
AA Mutation	p.Ala488Thr(p.A488T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664578:56664578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664023:56664023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664749:56664749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369167639
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664827:56664827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664293:56664293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664929:56664929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664359:56664359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769744617
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56663735:56663735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56663846:56663846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56663777:56663777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376886468
CDS Mutation	c.1422C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664266:56664266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664722:56664722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF835

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56663826:56663826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458His(p.R458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664090:56664090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109G>A
AA Mutation	p.Arg370His(p.R370H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000537055
Start	56664448:56664448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562824788
CDS Mutation	c.751G>A
AA Mutation	p.Glu251Lys(p.E251K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56663953:56663953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000537055
Start	56664263:56664263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776603650
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript