Colon Cancer: Gene >> CLCN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184346748:184346748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2555C>T
AA Mutation	p.Pro852Leu(p.P852L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184359071:184359071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760164094
CDS Mutation	c.124C>T
AA Mutation	p.Arg42Cys(p.R42C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184358041:184358041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536A>G
AA Mutation	p.Tyr179Cys(p.Y179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184357438:184357438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822C>A
AA Mutation	p.Asn274Lys(p.N274K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184346946:184346946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2491A>G
AA Mutation	p.Thr831Ala(p.T831A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184352059:184352059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2369T>C
AA Mutation	p.Ile790Thr(p.I790T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184346758:184346758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2545A>G
AA Mutation	p.Lys849Glu(p.K849E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184346709:184346709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2594G>A
AA Mutation	p.Ser865Asn(p.S865N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184361472:184361472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8C>T
AA Mutation	p.Ala3Val(p.A3V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265593
Start	184357680:184357680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712G>A
AA Mutation	p.Glu238Lys(p.E238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265593
Start	184354573:184354573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265593
Start	184359105:184359105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265593
Start	184358285:184358285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760319914
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265593
Start	184353278:184353278(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2000delC
AA Mutation	p.Pro667LeufsTer11(p.P667Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265593
Start	184353108:184353108(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2068delG
AA Mutation	p.Glu690ArgfsTer6(p.E690Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265593
Start	184355722:184355722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1142delC
AA Mutation	p.Pro381LeufsTer35(p.P381Lfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CLCN2

No Mutation Annotation!