Colon Cancer: Gene >> ZNF560

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467113:9467113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145243922
CDS Mutation	c.1834C>T
AA Mutation	p.Arg612Cys(p.R612C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9468082:9468082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>T
AA Mutation	p.Asp289Tyr(p.D289Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9474252:9474252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104G>T
AA Mutation	p.Arg35Ile(p.R35I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9470498:9470498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342T>G
AA Mutation	p.Ser114Arg(p.S114R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9469152:9469152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>A
AA Mutation	p.Leu189Ile(p.L189I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9470431:9470431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409G>A
AA Mutation	p.Asp137Asn(p.D137N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467248:9467248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142348936
CDS Mutation	c.1699G>A
AA Mutation	p.Ala567Thr(p.A567T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467256:9467256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267605824
CDS Mutation	c.1691G>A
AA Mutation	p.Arg564Gln(p.R564Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9468078:9468078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869A>C
AA Mutation	p.Lys290Thr(p.K290T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467668:9467668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771372963
CDS Mutation	c.1279G>A
AA Mutation	p.Ala427Thr(p.A427T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467601:9467601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Gly449Glu(p.G449E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9466725:9466725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2222A>G
AA Mutation	p.Lys741Arg(p.K741R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9466756:9466756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2191G>A
AA Mutation	p.Val731Met(p.V731M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467958:9467958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989C>G
AA Mutation	p.Thr330Ser(p.T330S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467985:9467985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962A>T
AA Mutation	p.Glu321Val(p.E321V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301480
Start	9471299:9471299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764745862
CDS Mutation	c.318A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301480
Start	9468062:9468062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000301480
Start	9467998:9467998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>T
AA Mutation	p.Glu317Ter(p.E317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF560

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467340:9467340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557447622
CDS Mutation	c.1607G>A
AA Mutation	p.Arg536Gln(p.R536Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9474288:9474288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>G
AA Mutation	p.Thr23Ser(p.T23S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9469696:9469696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>C
AA Mutation	p.Lys155Gln(p.K155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9466668:9466668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2279G>T
AA Mutation	p.Arg760Ile(p.R760I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9467424:9467424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523G>A
AA Mutation	p.Arg508Lys(p.R508K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9466771:9466771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2176G>T
AA Mutation	p.Asp726Tyr(p.D726Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301480
Start	9468330:9468330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>T
AA Mutation	p.Arg206Ile(p.R206I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301480
Start	9470456:9470456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301480
Start	9467660:9467660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000301480
Start	9467158:9467158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789G>T
AA Mutation	p.Glu597Ter(p.E597*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000301480
Start	9467662:9467662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285G>T
AA Mutation	p.Glu429Ter(p.E429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript