Colon Cancer: Gene >> ARHGEF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136708762:136708762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.836C>A
AA Mutation	p.Thr279Asn(p.T279N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136732117:136732117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717G>T
AA Mutation	p.Lys239Asn(p.K239N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136743648:136743648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>A
AA Mutation	p.Gly200Ser(p.G200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136681905:136681905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1543A>C
AA Mutation	p.Thr515Pro(p.T515P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136780803:136780803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>T
AA Mutation	p.Pro27Leu(p.P27L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136682804:136682804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433T>C
AA Mutation	p.Leu478Pro(p.L478P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136675049:136675049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993G>A
AA Mutation	p.Ala665Thr(p.A665T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136676642:136676642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771055558
CDS Mutation	c.1927G>C
AA Mutation	p.Glu643Gln(p.E643Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136747562:136747562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Val94Ile(p.V94I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136668066:136668066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368151602
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765Gln(p.R765Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136668137:136668137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2223A>C
AA Mutation	p.Glu741Asp(p.E741D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136676686:136676686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1883A>C
AA Mutation	p.Lys628Thr(p.K628T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136687941:136687941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236A>C
AA Mutation	p.Lys412Asn(p.K412N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250617
Start	136675089:136675089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1953T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250617
Start	136713356:136713356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250617
Start	136679649:136679649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250617
Start	136672103:136672103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2052C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250617
Start	136681903:136681903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1545A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000250617
Start	136685820:136685820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249C>T
AA Mutation	p.Gln417Ter(p.Q417*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000250617
Start	136681926:136681926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522G>T
AA Mutation	p.Glu508Ter(p.E508*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250617
Start	136680759:136680760(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1675dupA
AA Mutation	p.Thr559AsnfsTer7(p.T559Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136682835:136682835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402G>C
AA Mutation	p.Glu468Gln(p.E468Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136675034:136675034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2008G>A
AA Mutation	p.Ala670Thr(p.A670T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250617
Start	136780775:136780775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108A>C
AA Mutation	p.Lys36Asn(p.K36N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000250617
Start	136669493:136669493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2179G>T
AA Mutation	p.Glu727Ter(p.E727*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript