Colon Cancer: Gene >> CLCNKB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375679
Start	16056900:16056900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368764495
CDS Mutation	c.2048C>T
AA Mutation	p.Pro683Leu(p.P683L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375679
Start	16048537:16048537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909132
CDS Mutation	c.610G>A
AA Mutation	p.Ala204Thr(p.A204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375679
Start	16048527:16048527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600G>A
AA Mutation	p.Met200Ile(p.M200I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375679
Start	16051749:16051749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337T>G
AA Mutation	p.Phe446Cys(p.F446C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375679
Start	16051536:16051536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286T>G
AA Mutation	p.Ile429Ser(p.I429S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375679
Start	16053649:16053649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773177291
CDS Mutation	c.1633G>A
AA Mutation	p.Val545Met(p.V545M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375679
Start	16050576:16050576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147338414
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375679
Start	16048542:16048542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142452354
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375679
Start	16051802:16051802(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762878606
CDS Mutation	c.1395delG
AA Mutation	p.Tyr466MetfsTer13(p.Y466Mfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CLCNKB

No Mutation Annotation!