Colon Cancer: Gene >> ARHGAP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11188771:11188771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780455582
CDS Mutation	c.1034C>T
AA Mutation	p.Thr345Met(p.T345M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11139003:11139003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2785G>A
AA Mutation	p.Ala929Thr(p.A929T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11139153:11139153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2635C>T
AA Mutation	p.Arg879Trp(p.R879W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11664576:11664576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>T
AA Mutation	p.Gly85Cys(p.G85C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11664279:11664279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550G>A
AA Mutation	p.Asp184Asn(p.D184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11186274:11186274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1235G>T
AA Mutation	p.Arg412Met(p.R412M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11139116:11139116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2672C>T
AA Mutation	p.Ala891Val(p.A891V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11156605:11156605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831G>A
AA Mutation	p.Glu611Lys(p.E611K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11254613:11254613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683A>G
AA Mutation	p.Gln228Arg(p.Q228R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11664822:11664822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772160289
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11139022:11139022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2766G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11188878:11188878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11188863:11188863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11186312:11186312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1197G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11664760:11664760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779665222
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11178193:11178193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1536T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337414
Start	11664565:11664565(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.264delC
AA Mutation	p.Arg89GlyfsTer123(p.R89Gfs*123)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337414
Start	11186324:11186324(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1185delA
AA Mutation	p.Ala396ProfsTer8(p.A396Pfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11139494:11139494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2294G>C
AA Mutation	p.Arg765Thr(p.R765T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11144240:11144240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1916A>C
AA Mutation	p.Asp639Ala(p.D639A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337414
Start	11178150:11178150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579T>G
AA Mutation	p.Ser527Ala(p.S527A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337414
Start	11188824:11188824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981C>A
Mutation Classification	Silent
Feature Type	Transcript