Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF699

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9302431:9302431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776614133
CDS Mutation	c.122G>T
AA Mutation	p.Arg41Ile(p.R41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9296702:9296702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702T>G
AA Mutation	p.Phe234Leu(p.F234L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9295803:9295803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1601A>T
AA Mutation	p.Lys534Met(p.K534M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9295710:9295710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694G>A
AA Mutation	p.Gly565Glu(p.G565E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9295711:9295711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1693G>T
AA Mutation	p.Gly565Trp(p.G565W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9296671:9296671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733C>T
AA Mutation	p.Pro245Ser(p.P245S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9296421:9296421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983T>C
AA Mutation	p.Ile328Thr(p.I328T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9295708:9295708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696A>G
AA Mutation	p.Lys566Glu(p.K566E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9296087:9296087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1317A>C
AA Mutation	p.Lys439Asn(p.K439N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9297450:9297450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316T>C
AA Mutation	p.Ser106Pro(p.S106P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9295525:9295525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879C>A
AA Mutation	p.Pro627Thr(p.P627T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308650
Start	9295610:9295610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1794T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308650
Start	9296540:9296540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.864T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000308650
Start	9295804:9295804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600A>T
AA Mutation	p.Lys534Ter(p.K534*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000308650
Start	9295513:9295513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145027997
CDS Mutation	c.1891C>T
AA Mutation	p.Arg631Ter(p.R631*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF699

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9296664:9296664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740A>G
AA Mutation	p.Glu247Gly(p.E247G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9297360:9297360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406T>G
AA Mutation	p.Leu136Val(p.L136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308650
Start	9302431:9302431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776614133
CDS Mutation	c.122G>T
AA Mutation	p.Arg41Ile(p.R41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308650
Start	9296285:9296285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771715386
CDS Mutation	c.1119C>T
Mutation Classification	Silent
Feature Type	Transcript