Colon Cancer: Gene >> ATP8B3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1783241:1783241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3690G>T
AA Mutation	p.Glu1230Asp(p.E1230D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1790800:1790800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2335C>A
AA Mutation	p.Leu779Met(p.L779M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1790808:1790808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327C>T
AA Mutation	p.Ala776Val(p.A776V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1800317:1800317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543583339
CDS Mutation	c.1285G>A
AA Mutation	p.Val429Ile(p.V429I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1800419:1800419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183G>C
AA Mutation	p.Val395Leu(p.V395L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1790789:1790789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2346G>T
AA Mutation	p.Glu782Asp(p.E782D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1796779:1796779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374253006
CDS Mutation	c.1685G>A
AA Mutation	p.Arg562Gln(p.R562Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1800364:1800364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1238A>G
AA Mutation	p.Tyr413Cys(p.Y413C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1796768:1796768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749622913
CDS Mutation	c.1696C>T
AA Mutation	p.Arg566Cys(p.R566C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1808328:1808328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410T>C
AA Mutation	p.Val137Ala(p.V137A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1783186:1783186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777966827
CDS Mutation	c.3745C>T
AA Mutation	p.Arg1249Cys(p.R1249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1784926:1784926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3553T>C
AA Mutation	p.Ser1185Pro(p.S1185P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1800043:1800043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456C>A
AA Mutation	p.Leu486Met(p.L486M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1783197:1783197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3734C>A
AA Mutation	p.Ser1245Tyr(p.S1245Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000310127
Start	1785705:1785705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778738154
CDS Mutation	c.3157G>A
AA Mutation	p.Val1053Met(p.V1053M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310127
Start	1806681:1806681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310127
Start	1796745:1796745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310127
Start	1811707:1811707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310127
Start	1791796:1791796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2256C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310127
Start	1785178:1785178(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3513delC
AA Mutation	p.Thr1172ArgfsTer12(p.T1172Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000310127
Start	1800386:1800386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777333038
CDS Mutation	c.1216G>T
AA Mutation	p.Glu406Ter(p.E406*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000310127
Start	1805410:1805410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>T
AA Mutation	p.Glu290Ter(p.E290*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATP8B3

No Mutation Annotation!