Colon Cancer: Gene >> NHLRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369301
Start	113879594:113879594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>T
AA Mutation	p.Asp270Tyr(p.D270Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369301
Start	113903554:113903554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522A>C
AA Mutation	p.Asn508His(p.N508H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369301
Start	113904928:113904928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1816G>A
AA Mutation	p.Val606Met(p.V606M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369301
Start	113858540:113858540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191T>C
AA Mutation	p.Leu64Pro(p.L64P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369301
Start	113858594:113858594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245T>C
AA Mutation	p.Val82Ala(p.V82A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369301
Start	113898204:113898204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>T
AA Mutation	p.Lys378Asn(p.K378N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369301
Start	113901873:113901873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146402410
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369301
Start	113901732:113901732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369301
Start	113876672:113876672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369301
Start	113876621:113876621(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.432delT
AA Mutation	p.Met145TrpfsTer13(p.M145Wfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369301
Start	113902549:113902549(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1456delA
AA Mutation	p.Arg486GlyfsTer27(p.R486Gfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369301
Start	113903549:113903550(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1523dupA
AA Mutation	p.Asn508LysfsTer13(p.N508Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369301
Start	113902548:113902549(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1456dupA
AA Mutation	p.Arg486LysfsTer15(p.R486Kfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000369301
Start	113902470:113902470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NHLRC2

No Mutation Annotation!