Colon Cancer: Gene >> NCSTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294785
Start	160352108:160352108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.898G>A
AA Mutation	p.Ala300Thr(p.A300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294785
Start	160354253:160354253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144264818
CDS Mutation	c.1315G>A
AA Mutation	p.Val439Ile(p.V439I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294785
Start	160349561:160349561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327G>T
AA Mutation	p.Glu109Asp(p.E109D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294785
Start	160352178:160352178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200596888
CDS Mutation	c.968G>A
AA Mutation	p.Arg323His(p.R323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294785
Start	160344779:160344779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143C>A
AA Mutation	p.Ala48Asp(p.A48D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000294785
Start	160349646:160349646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Val138Ile(p.V138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294785
Start	160358169:160358169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294785
Start	160343409:160343409(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.17delG
AA Mutation	p.Gly6ValfsTer22(p.G6Vfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000294785
Start	160354223:160354223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771414318
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Ter(p.R429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000294785
Start	160350160:160350160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492G>A
AA Mutation	p.Trp164Ter(p.W164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NCSTN

No Mutation Annotation!