Colon Cancer: Gene >> RNASEL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182586631:182586631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176G>A
AA Mutation	p.Gly59Asp(p.G59D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182585472:182585472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335G>T
AA Mutation	p.Leu445Phe(p.L445F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182586766:182586766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766296817
CDS Mutation	c.41C>T
AA Mutation	p.Thr14Met(p.T14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182586469:182586469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>G
AA Mutation	p.Ser113Cys(p.S113C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182586502:182586502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305C>T
AA Mutation	p.Ala102Val(p.A102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367559
Start	182575470:182575470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763696156
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367559
Start	182586525:182586525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768816440
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367559
Start	182586165:182586165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148741721
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367559
Start	182585774:182585774(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1033delG
AA Mutation	p.Ala345GlnfsTer3(p.A345Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367559
Start	182576365:182576365(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1930delA
AA Mutation	p.Met644Ter(p.M644*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367559
Start	182585661:182585661(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1146delG
AA Mutation	p.Phe383SerfsTer7(p.F383Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000367559
Start	182576383:182576383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912G>T
AA Mutation	p.Glu638Ter(p.E638*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000367559
Start	182585963:182585963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844G>T
AA Mutation	p.Glu282Ter(p.E282*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367559
Start	182576343:182576344(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1951dupA
AA Mutation	p.Arg651LysfsTer11(p.R651Kfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367559
Start	182576364:182576365(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1930dupA
AA Mutation	p.Met644AsnfsTer3(p.M644Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNASEL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182584110:182584110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1537G>A
AA Mutation	p.Asp513Asn(p.D513N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367559
Start	182576358:182576358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1937A>C
AA Mutation	p.Lys646Thr(p.K646T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367559
Start	182576387:182576387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1908T>G
AA Mutation	p.Ile636Met(p.I636M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript