Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RALGAPA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20524451:20524451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3855G>T
AA Mutation	p.Glu1285Asp(p.E1285D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20619369:20619369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747438948
CDS Mutation	c.1447C>T
AA Mutation	p.Arg483Cys(p.R483C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20531787:20531787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763690497
CDS Mutation	c.3482C>T
AA Mutation	p.Ala1161Val(p.A1161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20591311:20591311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2207T>C
AA Mutation	p.Val736Ala(p.V736A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20412084:20412084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5560G>A
AA Mutation	p.Glu1854Lys(p.E1854K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20531734:20531734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3535C>A
AA Mutation	p.His1179Asn(p.H1179N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20495263:20495263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5221G>T
AA Mutation	p.Gly1741Trp(p.G1741W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20526257:20526257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761666923
CDS Mutation	c.3688G>A
AA Mutation	p.Ala1230Thr(p.A1230T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20526308:20526308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3637T>C
AA Mutation	p.Ser1213Pro(p.S1213P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20513180:20513180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777380984
CDS Mutation	c.4189A>G
AA Mutation	p.Ile1397Val(p.I1397V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20472874:20472874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5450A>G
AA Mutation	p.Asn1817Ser(p.N1817S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20620505:20620505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359A>T
AA Mutation	p.Glu453Asp(p.E453D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20637465:20637465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>T
AA Mutation	p.Asp235Tyr(p.D235Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20629442:20629442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373215034
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385Gln(p.R385Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000202677
Start	20495275:20495275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5209C>A
AA Mutation	p.Leu1737Ile(p.L1737I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20513231:20513231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4138G>A
AA Mutation	p.Ala1380Thr(p.A1380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20412076:20412076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5568C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20616153:20616153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1578A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20524472:20524472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184808613
CDS Mutation	c.3834C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20589316:20589316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2391T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20546737:20546737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762230375
CDS Mutation	c.3252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20616180:20616180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367939584
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20573022:20573022(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2754delG
AA Mutation	p.Ser919AlafsTer24(p.S919Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20513020:20513020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4349delG
AA Mutation	p.Gly1450AspfsTer10(p.G1450Dfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20616084:20616084(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1647delT
AA Mutation	p.Phe549LeufsTer4(p.F549Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20512885:20512885(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4484delT
AA Mutation	p.Leu1495ArgfsTer46(p.L1495Rfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20571496:20571496(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3118delT
AA Mutation	p.Tyr1040ThrfsTer3(p.Y1040Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000202677
Start	20639883:20639883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>T
AA Mutation	p.Glu190Ter(p.E190*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20605372:20605373(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1840_1841insTCTTTTCCTTTTGTTC
AA Mutation	p.Tyr614PhefsTer14(p.Y614Ffs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000202677
Start	20616041:20616041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000202677
Start	20605370:20605371(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1842_1843insTTA
AA Mutation	p.Tyr614_Ile615insLeu(p.Y614_I615insL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RALGAPA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20520965:20520965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4036C>A
AA Mutation	p.Gln1346Lys(p.Q1346K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20495141:20495141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5343C>A
AA Mutation	p.Phe1781Leu(p.F1781L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20503388:20503388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200369501
CDS Mutation	c.5171G>A
AA Mutation	p.Arg1724Gln(p.R1724Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20605191:20605191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2022G>T
AA Mutation	p.Lys674Asn(p.K674N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20511307:20511307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4875G>T
AA Mutation	p.Leu1625Phe(p.L1625F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20535767:20535767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3451G>A
AA Mutation	p.Glu1151Lys(p.E1151K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20584945:20584945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577169706
CDS Mutation	c.2450G>A
AA Mutation	p.Arg817Gln(p.R817Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000202677
Start	20616048:20616048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1683G>T
AA Mutation	p.Lys561Asn(p.K561N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202677
Start	20635574:20635574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202677
Start	20640794:20640795(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.456dupT
AA Mutation	p.Ala153CysfsTer28(p.A153Cfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript