Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ABCC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16056120:16056120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502G>A
AA Mutation	p.Arg501Gln(p.R501Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16068195:16068195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751292519
CDS Mutation	c.1717G>A
AA Mutation	p.Glu573Lys(p.E573K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16111382:16111382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2879T>G
AA Mutation	p.Leu960Arg(p.L960R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16115018:16115018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3332C>A
AA Mutation	p.Ala1111Asp(p.A1111D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16141258:16141258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4573G>A
AA Mutation	p.Ala1525Thr(p.A1525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16131817:16131817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765498811
CDS Mutation	c.3848C>T
AA Mutation	p.Pro1283Leu(p.P1283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16114895:16114895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3209G>A
AA Mutation	p.Gly1070Glu(p.G1070E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16106796:16106796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768011444
CDS Mutation	c.2794G>A
AA Mutation	p.Ala932Thr(p.A932T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16045897:16045897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200520366
CDS Mutation	c.1102G>A
AA Mutation	p.Val368Met(p.V368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16131925:16131925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3956G>T
AA Mutation	p.Gly1319Val(p.G1319V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000399410
Start	16090406:16090406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2462C>T
AA Mutation	p.Thr821Met(p.T821M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16079410:16079410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766665700
CDS Mutation	c.2047G>A
AA Mutation	p.Gly683Arg(p.G683R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16106797:16106797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375097324
CDS Mutation	c.2795C>T
AA Mutation	p.Ala932Val(p.A932V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16044589:16044589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949T>G
AA Mutation	p.Leu317Val(p.L317V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16102633:16102633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751066573
CDS Mutation	c.2651C>T
AA Mutation	p.Thr884Met(p.T884M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16056269:16056269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651T>G
AA Mutation	p.Phe551Val(p.F551V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16124875:16124875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3677G>A
AA Mutation	p.Ser1226Asn(p.S1226N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16044623:16044623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983G>A
AA Mutation	p.Ser328Asn(p.S328N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16141207:16141207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4522T>C
AA Mutation	p.Tyr1508His(p.Y1508H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16090525:16090525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45517537
CDS Mutation	c.2581G>A
AA Mutation	p.Ala861Thr(p.A861T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16136485:16136485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4133T>C
AA Mutation	p.Val1378Ala(p.V1378A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16076335:16076335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756498834
CDS Mutation	c.1922C>T
AA Mutation	p.Thr641Met(p.T641M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16079406:16079406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2043C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16068275:16068275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16111461:16111461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45607431
CDS Mutation	c.2958T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16068209:16068209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16048180:16048180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16048213:16048213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371886235
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16106861:16106861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372453304
CDS Mutation	c.2859G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16136537:16136537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200975492
CDS Mutation	c.4185G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16122031:16122031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16122133:16122133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759822263
CDS Mutation	c.3549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16111539:16111539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3036G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16071683:16071683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1866T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16114843:16114843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3157C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399410
Start	16016541:16016541(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.538delT
AA Mutation	p.Ser180ProfsTer48(p.S180Pfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399410
Start	16141214:16141214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4532delC
AA Mutation	p.Pro1511HisfsTer54(p.P1511Hfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000399410
Start	16124906:16124906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3708C>G
AA Mutation	p.Tyr1236Ter(p.Y1236*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000399410
Start	16071660:16071661(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1843_1844insTGA
AA Mutation	p.Arg615delinsLeuSer(p.R615delinsLS)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ABCC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16122150:16122150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3566A>G
AA Mutation	p.Tyr1189Cys(p.Y1189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16068177:16068177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545772203
CDS Mutation	c.1699G>A
AA Mutation	p.Val567Ile(p.V567I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16048239:16048239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316C>G
AA Mutation	p.Thr439Arg(p.T439R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16044668:16044668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749166736
CDS Mutation	c.1028C>T
AA Mutation	p.Pro343Leu(p.P343L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16115029:16115029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371062976
CDS Mutation	c.3343G>A
AA Mutation	p.Ala1115Thr(p.A1115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16134407:16134407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201020041
CDS Mutation	c.4024C>T
AA Mutation	p.Arg1342Trp(p.R1342W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399410
Start	16016558:16016558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552T>G
AA Mutation	p.Ile184Met(p.I184M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16138442:16138442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202222707
CDS Mutation	c.4371G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399410
Start	16044519:16044519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879G>A
Mutation Classification	Silent
Feature Type	Transcript