Colon Cancer: Gene >> ATP11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112842309:112842309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1739C>A
AA Mutation	p.Ser580Tyr(p.S580Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112862510:112862510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140812688
CDS Mutation	c.2926G>A
AA Mutation	p.Ala976Thr(p.A976T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000375645
Start	112836180:112836180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634T>A
AA Mutation	p.Phe545Tyr(p.F545Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112819314:112819314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778305375
CDS Mutation	c.581C>T
AA Mutation	p.Ala194Val(p.A194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112862555:112862555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2971A>G
AA Mutation	p.Thr991Ala(p.T991A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112856047:112856047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2380G>A
AA Mutation	p.Val794Met(p.V794M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112785204:112785204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769716430
CDS Mutation	c.109G>A
AA Mutation	p.Ala37Thr(p.A37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112824362:112824362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809G>A
AA Mutation	p.Gly270Glu(p.G270E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112833010:112833010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745600009
CDS Mutation	c.1546G>A
AA Mutation	p.Glu516Lys(p.E516K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112824418:112824418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865G>A
AA Mutation	p.Val289Met(p.V289M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112826770:112826770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100C>T
AA Mutation	p.Thr367Met(p.T367M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112862508:112862508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2924A>G
AA Mutation	p.Asp975Gly(p.D975G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112832935:112832935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471G>T
AA Mutation	p.Gly491Cys(p.G491C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112854485:112854485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770429974
CDS Mutation	c.2198C>T
AA Mutation	p.Thr733Met(p.T733M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112826816:112826816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147148624
CDS Mutation	c.1146C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112858269:112858269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772564438
CDS Mutation	c.2646C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112823405:112823405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112831542:112831542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201730815
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112875863:112875863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3249G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112856043:112856043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78821510
CDS Mutation	c.2376C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112833009:112833009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112862539:112862539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757038675
CDS Mutation	c.2955C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375645
Start	112832956:112832956(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1497delG
AA Mutation	p.Lys500AsnfsTer27(p.K500Nfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375645
Start	112823406:112823406(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.789delT
AA Mutation	p.Phe263LeufsTer15(p.F263Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000375645
Start	112851139:112851139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912C>T
AA Mutation	p.Arg638Ter(p.R638*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATP11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375645
Start	112833017:112833017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553T>C
AA Mutation	p.Val518Ala(p.V518A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112819903:112819903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765223400
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112862539:112862539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757038675
CDS Mutation	c.2955C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112873620:112873620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375645
Start	112834655:112834655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770395954
CDS Mutation	c.1626C>T
Mutation Classification	Silent
Feature Type	Transcript