Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RASGRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79035142:79035142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751054636
CDS Mutation	c.947C>T
AA Mutation	p.Thr316Met(p.T316M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79001703:79001703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2582C>A
AA Mutation	p.Ser861Tyr(p.S861Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78998780:78998780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770002588
CDS Mutation	c.2840G>A
AA Mutation	p.Arg947His(p.R947H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046858:79046858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770085797
CDS Mutation	c.766G>A
AA Mutation	p.Val256Met(p.V256M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79025387:79025387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469G>A
AA Mutation	p.Arg490Gln(p.R490Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79025424:79025424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432C>T
AA Mutation	p.Arg478Cys(p.R478C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79003936:79003936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363C>T
AA Mutation	p.Ala788Val(p.A788V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79049561:79049561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79006309:79006309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1991G>A
AA Mutation	p.Arg664His(p.R664H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78973332:78973332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761559564
CDS Mutation	c.3631G>A
AA Mutation	p.Gly1211Ser(p.G1211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79090476:79090476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23A>G
AA Mutation	p.Asn8Ser(p.N8S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79090483:79090483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16C>T
AA Mutation	p.Arg6Trp(p.R6W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78998781:78998781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368623142
CDS Mutation	c.2839C>T
AA Mutation	p.Arg947Cys(p.R947C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79058459:79058459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406C>T
AA Mutation	p.His136Tyr(p.H136Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79004053:79004053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748449776
CDS Mutation	c.2246C>T
AA Mutation	p.Ser749Leu(p.S749L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000419573
Start	79049496:79049496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624G>C
AA Mutation	p.Lys208Asn(p.K208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78971924:78971924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781050482
CDS Mutation	c.3671T>G
AA Mutation	p.Ile1224Ser(p.I1224S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79049560:79049560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780918719
CDS Mutation	c.560G>A
AA Mutation	p.Arg187His(p.R187H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79006346:79006346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1954A>G
AA Mutation	p.Ser652Gly(p.S652G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79049551:79049551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569C>A
AA Mutation	p.Ser190Tyr(p.S190Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79004126:79004126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754245001
CDS Mutation	c.2173G>A
AA Mutation	p.Gly725Ser(p.G725S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79012492:79012492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747677216
CDS Mutation	c.1862G>A
AA Mutation	p.Ser621Asn(p.S621N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79004001:79004001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142558192
CDS Mutation	c.2298C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78990198:78990198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79032207:79032207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754567427
CDS Mutation	c.1068C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78985139:78985139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542075208
CDS Mutation	c.3330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79064464:79064464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201439198
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78991786:78991786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147869279
CDS Mutation	c.3084C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79006317:79006317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761805791
CDS Mutation	c.1983G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78999909:78999909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2628C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79027775:79027775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79003977:79003977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2322C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79027805:79027805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770607726
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79017863:79017863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756158411
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79046772:79046772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754755775
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78991744:78991744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760253908
CDS Mutation	c.3126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79090337:79090337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000419573
Start	79035193:79035193(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.896delT
AA Mutation	p.Leu299TyrfsTer9(p.L299Yfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000419573
Start	78990263:78990263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3190G>T
AA Mutation	p.Gly1064Ter(p.G1064*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000419573
Start	78971919:78971919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3676C>T
AA Mutation	p.Arg1226Ter(p.R1226*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000419573
Start	78998737:78998737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2883G>A
AA Mutation	p.Trp961Ter(p.W961*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RASGRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046909:79046909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Cys(p.R239C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79046822:79046822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78971910:78971910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561370237
CDS Mutation	c.3685C>T
AA Mutation	p.Arg1229Cys(p.R1229C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	78991769:78991769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3101T>G
AA Mutation	p.Phe1034Cys(p.F1034C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000419573
Start	79032146:79032146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129T>C
AA Mutation	p.Phe377Leu(p.F377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78995746:78995746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3069G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	78985016:78985016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3453C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419573
Start	79046781:79046781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000419573
Start	79015326:79015326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1826+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript