Colon Cancer: Gene >> KCNJ5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911406:128911406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372447456
CDS Mutation	c.133G>A
AA Mutation	p.Glu45Lys(p.E45K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911395:128911395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139073333
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911383:128911383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110C>T
AA Mutation	p.Thr37Ile(p.T37I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911670:128911670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>A
AA Mutation	p.Leu133Ile(p.L133I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128912156:128912156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883C>T
AA Mutation	p.His295Tyr(p.H295Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911427:128911427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154C>T
AA Mutation	p.Arg52Cys(p.R52C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911889:128911889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750424299
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128912058:128912058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785A>G
AA Mutation	p.Asp262Gly(p.D262G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000338350
Start	128911334:128911334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61G>A
AA Mutation	p.Asp21Asn(p.D21N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338350
Start	128911363:128911363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201886526
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338350
Start	128911447:128911447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNJ5

No Mutation Annotation!