Colon Cancer: Gene >> NISCH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52489356:52489356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3134A>T
AA Mutation	p.Glu1045Val(p.E1045V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52488581:52488581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3089G>A
AA Mutation	p.Gly1030Asp(p.G1030D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52472309:52472309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580G>A
AA Mutation	p.Gly194Ser(p.G194S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52457859:52457859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110T>C
AA Mutation	p.Val37Ala(p.V37A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52488125:52488125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2633A>G
AA Mutation	p.Asn878Ser(p.N878S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52489523:52489523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370428956
CDS Mutation	c.3301G>A
AA Mutation	p.Glu1101Lys(p.E1101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52488448:52488448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2956G>A
AA Mutation	p.Val986Met(p.V986M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000345716
Start	52490831:52490831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574046395
CDS Mutation	c.3740C>T
AA Mutation	p.Thr1247Met(p.T1247M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52488481:52488481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372817454
CDS Mutation	c.2989G>A
AA Mutation	p.Val997Ile(p.V997I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52491944:52491944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3977G>T
AA Mutation	p.Gly1326Val(p.G1326V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52478537:52478537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754670090
CDS Mutation	c.1262G>A
AA Mutation	p.Arg421Gln(p.R421Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52488166:52488166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145350144
CDS Mutation	c.2674C>T
AA Mutation	p.Arg892Cys(p.R892C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52478179:52478179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070T>A
AA Mutation	p.Ile357Asn(p.I357N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52458665:52458665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140213598
CDS Mutation	c.181G>A
AA Mutation	p.Val61Ile(p.V61I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52490822:52490822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3731T>G
AA Mutation	p.Phe1244Cys(p.F1244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52491404:52491404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767487374
CDS Mutation	c.3795G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52487259:52487259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1767C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52487421:52487421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52471908:52471908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146742349
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52489543:52489543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200619504
CDS Mutation	c.3321G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52458799:52458799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200818525
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52492011:52492011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4044G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345716
Start	52488539:52488539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3051delC
AA Mutation	p.Thr1019ArgfsTer140(p.T1019Rfs*140)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NISCH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345716
Start	52488479:52488479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528293970
CDS Mutation	c.2987G>A
AA Mutation	p.Arg996His(p.R996H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52484616:52484616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1632G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52488549:52488549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3057G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52492269:52492269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345716
Start	52458697:52458697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213T>C
Mutation Classification	Silent
Feature Type	Transcript