Colon Cancer: Gene >> ARHGAP12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31908333:31908333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31839687:31839687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321T>C
AA Mutation	p.Cys441Arg(p.C441R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31810729:31810729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1970A>C
AA Mutation	p.Asn657Thr(p.N657T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31826382:31826382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452G>T
AA Mutation	p.Lys484Asn(p.K484N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31854179:31854179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976A>G
AA Mutation	p.Ser326Gly(p.S326G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31908530:31908530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326A>C
AA Mutation	p.Lys109Thr(p.K109T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31807806:31807806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393G>A
AA Mutation	p.Arg798Gln(p.R798Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31810726:31810726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1973T>C
AA Mutation	p.Leu658Pro(p.L658P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31812774:31812774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1884A>C
AA Mutation	p.Lys628Asn(p.K628N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31854101:31854101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054C>T
AA Mutation	p.His352Tyr(p.H352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344936
Start	31854171:31854171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344936
Start	31852571:31852571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344936
Start	31908580:31908580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344936
Start	31807814:31807814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2385G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000344936
Start	31831802:31831802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765342639
CDS Mutation	c.1387-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31808668:31808668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2347C>A
AA Mutation	p.Leu783Ile(p.L783I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31908284:31908284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572C>A
AA Mutation	p.Thr191Asn(p.T191N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31817870:31817870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649G>T
AA Mutation	p.Gly550Val(p.G550V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31820399:31820399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1620G>T
AA Mutation	p.Lys540Asn(p.K540N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344936
Start	31861624:31861624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.719C>A
AA Mutation	p.Ser240Tyr(p.S240Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000344936
Start	31843559:31843559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198G>T
AA Mutation	p.Glu400Ter(p.E400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript