Colon Cancer: Gene >> KCNS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17932398:17932398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150320186
CDS Mutation	c.1390G>A
AA Mutation	p.Asp464Asn(p.D464N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931606:17931606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537401566
CDS Mutation	c.598G>A
AA Mutation	p.Val200Met(p.V200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931529:17931529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>T
AA Mutation	p.Arg174Ile(p.R174I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931378:17931378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76178253
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Cys(p.R124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931712:17931712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704G>A
AA Mutation	p.Gly235Glu(p.G235E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931255:17931255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247T>G
AA Mutation	p.Tyr83Asp(p.Y83D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931735:17931735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>T
AA Mutation	p.Ala243Ser(p.A243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17932206:17932206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Leu400Phe(p.L400F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17932041:17932041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143152428
CDS Mutation	c.1033G>A
AA Mutation	p.Val345Met(p.V345M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17932397:17932397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776349440
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17931692:17931692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779009471
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17931875:17931875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17931632:17931632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140824188
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17931557:17931557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201603883
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17931941:17931941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304101
Start	17931263:17931263(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.258delG
AA Mutation	p.Lys87SerfsTer54(p.K87Sfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000304101
Start	17931760:17931760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752G>A
AA Mutation	p.Trp251Ter(p.W251*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KCNS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304101
Start	17931612:17931612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604A>T
AA Mutation	p.Met202Leu(p.M202L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304101
Start	17931632:17931632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140824188
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript