Colon Cancer: Gene >> NHLRC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39042109:39042109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390C>A
AA Mutation	p.Phe130Leu(p.F130L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39039642:39039642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316A>G
AA Mutation	p.Thr106Ala(p.T106A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39047102:39047102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741G>T
AA Mutation	p.Trp247Cys(p.W247C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39047843:39047843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961G>A
AA Mutation	p.Ala321Thr(p.A321T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39044176:39044176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673G>A
AA Mutation	p.Gly225Ser(p.G225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379600
Start	39038721:39038721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82C>T
AA Mutation	p.Pro28Ser(p.P28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39047855:39047855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>C
AA Mutation	p.Ala325Pro(p.A325P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379600
Start	39038672:39038672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379600
Start	39047880:39047880(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1002delA
AA Mutation	p.Lys334AsnfsTer5(p.K334Nfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379600
Start	39042176:39042176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.462delA
AA Mutation	p.Gly155AlafsTer4(p.G155Afs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379600
Start	39042125:39042125(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.411delA
AA Mutation	p.Lys137AsnfsTer22(p.K137Nfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NHLRC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39039584:39039584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258G>T
AA Mutation	p.Lys86Asn(p.K86N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379600
Start	39039172:39039172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121A>G
AA Mutation	p.Thr41Ala(p.T41A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000379600
Start	39047840:39047840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.958G>T
AA Mutation	p.Gly320Ter(p.G320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript