Colon Cancer: Gene >> ARHGAP26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	142932055:142932055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037T>C
AA Mutation	p.Val346Ala(p.V346A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	142770783:142770783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22T>C
AA Mutation	p.Phe8Leu(p.F8L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	143207365:143207365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2156G>T
AA Mutation	p.Arg719Leu(p.R719L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	143041824:143041824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368631485
CDS Mutation	c.1219G>A
AA Mutation	p.Glu407Lys(p.E407K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274498
Start	143207309:143207309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2100G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274498
Start	143207231:143207231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201177393
CDS Mutation	c.2022G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274498
Start	142901982:142901982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773011288
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274498
Start	143207339:143207339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2130T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274498
Start	143014091:143014091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000274498
Start	143207198:143207198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1994delC
AA Mutation	p.Pro665ArgfsTer135(p.P665Rfs*135)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000274498
Start	143037252:143037252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201G>T
AA Mutation	p.Glu401Ter(p.E401*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000274498
Start	143134106:143134106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGAP26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	142903550:142903550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	143054442:143054442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289C>G
AA Mutation	p.Pro430Arg(p.P430R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	143214059:143214059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327C>T
AA Mutation	p.Ser776Leu(p.S776L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274498
Start	143057710:143057710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501C>T
AA Mutation	p.Arg501Trp(p.R501W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript