Colon Cancer: Gene >> SNRPN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24978428:24978428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707G>A
AA Mutation	p.Arg236His(p.R236H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24975395:24975395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41A>G
AA Mutation	p.Asp14Gly(p.D14G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24976986:24976986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377G>T
AA Mutation	p.Gly126Val(p.G126V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24977827:24977827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775190561
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346403
Start	24975509:24975509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155A>C
AA Mutation	p.Lys52Thr(p.K52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24975377:24975377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23A>G
AA Mutation	p.Lys8Arg(p.K8R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24977848:24977848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24978261:24978261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628G>T
AA Mutation	p.Gly210Trp(p.G210W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346403
Start	24978281:24978281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746441330
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346403
Start	24978287:24978287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346403
Start	24976405:24976405(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.261delC
AA Mutation	p.Asp89IlefsTer53(p.D89Ifs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346403
Start	24978297:24978297(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.668delC
AA Mutation	p.Pro223LeufsTer39(p.P223Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SNRPN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346403
Start	24975394:24975394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40G>A
AA Mutation	p.Asp14Asn(p.D14N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript