Colon Cancer: Gene >> ATP2A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3942685:3942685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1466G>A
AA Mutation	p.Arg489Gln(p.R489Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3941507:3941507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1693G>A
AA Mutation	p.Ala565Thr(p.A565T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3947512:3947512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781334265
CDS Mutation	c.974G>A
AA Mutation	p.Arg325His(p.R325H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3937528:3937528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2209G>C
AA Mutation	p.Asp737His(p.D737H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3925397:3925397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766610781
CDS Mutation	c.3113C>T
AA Mutation	p.Pro1038Leu(p.P1038L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3928667:3928667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2976G>A
AA Mutation	p.Met992Ile(p.M992I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3951377:3951377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772945810
CDS Mutation	c.337G>A
AA Mutation	p.Glu113Lys(p.E113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3944739:3944739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143239393
CDS Mutation	c.1252G>A
AA Mutation	p.Ala418Thr(p.A418T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3947657:3947657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>T
AA Mutation	p.Gly277Cys(p.G277C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3944760:3944760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231G>A
AA Mutation	p.Val411Met(p.V411M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3937582:3937582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2155G>A
AA Mutation	p.Ala719Thr(p.A719T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3950717:3950717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3950718:3950718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3951647:3951647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140787007
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3936457:3936457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2334G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3944749:3944749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3947571:3947571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777538493
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000352011
Start	3941261:3941261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810C>T
AA Mutation	p.Arg604Ter(p.R604*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATP2A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3950768:3950768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Asp157Asn(p.D157N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352011
Start	3941633:3941633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1567G>A
AA Mutation	p.Glu523Lys(p.E523K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3944749:3944749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3941463:3941463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756412106
CDS Mutation	c.1737C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352011
Start	3943445:3943445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761171240
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript