Colon Cancer: Gene >> RASAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113114806:113114806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202023606
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392His(p.R392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113115244:113115244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1024C>A
AA Mutation	p.Arg342Ser(p.R342S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113104267:113104267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1859G>A
AA Mutation	p.Arg620His(p.R620H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113112123:113112123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446Gln(p.R446Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113114900:113114900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081C>T
AA Mutation	p.Pro361Ser(p.P361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113112147:113112147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438His(p.R438H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113104241:113104241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1885G>A
AA Mutation	p.Ala629Thr(p.A629T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113105758:113105758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1783C>T
AA Mutation	p.Leu595Phe(p.L595F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113116020:113116020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531834126
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Cys(p.R255C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113115942:113115942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841C>T
AA Mutation	p.Pro281Ser(p.P281S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113115737:113115737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901T>C
AA Mutation	p.Cys301Arg(p.C301R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261729
Start	113104200:113104200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1926C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261729
Start	113100052:113100052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2292C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261729
Start	113099986:113099986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769890741
CDS Mutation	c.2358C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261729
Start	113105723:113105723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261729
Start	113127870:113127870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114458989
CDS Mutation	c.240C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RASAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113112193:113112193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267G>A
AA Mutation	p.Val423Met(p.V423M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261729
Start	113119167:113119167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603G>T
AA Mutation	p.Trp201Cys(p.W201C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261729
Start	113115218:113115218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773166556
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript