Colon Cancer: Gene >> ABCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95234639:95234639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502G>A
AA Mutation	p.Val168Ile(p.V168I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95206542:95206542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763493372
CDS Mutation	c.1151G>A
AA Mutation	p.Arg384Gln(p.R384Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95178049:95178049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588G>T
AA Mutation	p.Asp530Tyr(p.D530Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95209498:95209498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721A>G
AA Mutation	p.Met241Val(p.M241V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95188467:95188467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339G>A
AA Mutation	p.Val447Met(p.V447M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376887
Start	95075549:95075549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769663620
CDS Mutation	c.2689C>T
AA Mutation	p.Arg897Trp(p.R897W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95247083:95247083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198A>T
AA Mutation	p.Lys66Asn(p.K66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95186743:95186743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503G>T
AA Mutation	p.Lys501Asn(p.K501N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95074300:95074300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750954023
CDS Mutation	c.2831C>T
AA Mutation	p.Thr944Met(p.T944M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95044329:95044329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3566G>T
AA Mutation	p.Arg1189Met(p.R1189M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95209549:95209549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>A
AA Mutation	p.Ala224Thr(p.A224T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95161324:95161324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2320G>A
AA Mutation	p.Ala774Thr(p.A774T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95178063:95178063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574T>C
AA Mutation	p.Leu525Pro(p.L525P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95021605:95021605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550257734
CDS Mutation	c.3948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95166203:95166203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775937284
CDS Mutation	c.1989A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95234619:95234619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.522T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95021590:95021590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768473583
CDS Mutation	c.3963C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95021674:95021674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95164395:95164395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95247037:95247037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95170583:95170583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1773T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95188492:95188492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150945397
CDS Mutation	c.1314C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376887
Start	95083178:95083178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2648delT
AA Mutation	p.Leu883TrpfsTer7(p.L883Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376887
Start	95161322:95161323(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2321_2322insAAGACATACT
AA Mutation	p.Thr775ArgfsTer21(p.T775Rfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000376887
Start	95206634:95206657(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1036_1059delATCACAGCCAGCCGCGTGTTCGTG
AA Mutation	p.Ile346_Val353del(p.I346_V353del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ABCC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376887
Start	95234735:95234735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>A
AA Mutation	p.Ala136Thr(p.A136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376887
Start	95071665:95071665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3207A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000376887
Start	95186893:95186893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1354-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript