Colon Cancer: Gene >> ATP2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89621590:89621590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546A>G
AA Mutation	p.Thr516Ala(p.T516A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89642196:89642196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368G>A
AA Mutation	p.Gly123Asp(p.G123D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89616833:89616833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2036T>C
AA Mutation	p.Val679Ala(p.V679A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89621652:89621652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1484A>G
AA Mutation	p.Lys495Arg(p.K495R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89610013:89610013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376575805
CDS Mutation	c.2366G>A
AA Mutation	p.Arg789His(p.R789H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89611343:89611343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2097G>T
AA Mutation	p.Arg699Ser(p.R699S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89620207:89620207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368317255
CDS Mutation	c.1621G>A
AA Mutation	p.Val541Ile(p.V541I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89604169:89604169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570457928
CDS Mutation	c.2620G>A
AA Mutation	p.Ala874Thr(p.A874T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89616953:89616953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1916C>T
AA Mutation	p.Pro639Leu(p.P639L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89599192:89599192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3276G>T
AA Mutation	p.Glu1092Asp(p.E1092D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89591228:89591228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3419C>T
AA Mutation	p.Ser1140Leu(p.S1140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89601364:89601364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3130T>C
AA Mutation	p.Ser1044Pro(p.S1044P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89603113:89603113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2990G>T
AA Mutation	p.Arg997Ile(p.R997I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89624260:89624260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267G>A
AA Mutation	p.Gly423Arg(p.G423R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89599167:89599167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746094247
CDS Mutation	c.3301C>T
AA Mutation	p.Arg1101Trp(p.R1101W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89611253:89611253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2187A>T
AA Mutation	p.Glu729Asp(p.E729D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428670
Start	89655881:89655881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199899576
CDS Mutation	c.6C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428670
Start	89599153:89599153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428670
Start	89626503:89626503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428670
Start	89621600:89621600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1536C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000428670
Start	89655748:89655748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Ter(p.R47*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATP2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89611209:89611209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2231G>A
AA Mutation	p.Arg744Gln(p.R744Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89621725:89621725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1411G>A
AA Mutation	p.Ala471Thr(p.A471T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89620038:89620038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1790G>A
AA Mutation	p.Arg597Gln(p.R597Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000428670
Start	89655700:89655700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187T>G
AA Mutation	p.Leu63Val(p.L63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428670
Start	89630521:89630521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000428670
Start	89642202:89642202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362C>A
AA Mutation	p.Ser121Ter(p.S121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript