Colon Cancer: Gene >> ARHGAP15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143624262:143624262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749157476
CDS Mutation	c.1133C>T
AA Mutation	p.Ala378Val(p.A378V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143767996:143767996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758104156
CDS Mutation	c.1252G>A
AA Mutation	p.Ala418Thr(p.A418T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143250582:143250582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>A
AA Mutation	p.Ser152Arg(p.S152R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143435655:143435655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375193013
CDS Mutation	c.529A>G
AA Mutation	p.Ile177Val(p.I177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143624242:143624242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113C>A
AA Mutation	p.Phe371Leu(p.F371L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143155638:143155638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>A
AA Mutation	p.Gly50Arg(p.G50R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143250573:143250573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447A>C
AA Mutation	p.Glu149Asp(p.E149D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143155498:143155498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8A>C
AA Mutation	p.Lys3Thr(p.K3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143155570:143155570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80G>C
AA Mutation	p.Arg27Thr(p.R27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143155521:143155521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140767178
CDS Mutation	c.31G>A
AA Mutation	p.Val11Met(p.V11M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295095
Start	143624143:143624143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295095
Start	143519324:143519324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752498477
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295095
Start	143487407:143487407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200906734
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295095
Start	143703474:143703474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295095
Start	143250594:143250594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295095
Start	143155637:143155637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752676733
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143768063:143768063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781102282
CDS Mutation	c.1319G>A
AA Mutation	p.Arg440Gln(p.R440Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295095
Start	143437022:143437022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683C>A
AA Mutation	p.Pro228Gln(p.P228Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000295095
Start	143436923:143436923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584C>A
AA Mutation	p.Ser195Ter(p.S195*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript