Colon Cancer: Gene >> SLC34A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676469:25676469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780836430
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598His(p.R598H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25674380:25674380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301C>A
AA Mutation	p.Ser434Tyr(p.S434Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676313:25676313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637G>A
AA Mutation	p.Gly546Asp(p.G546D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676718:25676718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2042C>T
AA Mutation	p.Ser681Leu(p.S681L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676595:25676595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374537882
CDS Mutation	c.1919G>A
AA Mutation	p.Arg640His(p.R640H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676427:25676427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758313049
CDS Mutation	c.1751C>T
AA Mutation	p.Pro584Leu(p.P584L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25662528:25662528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>A
AA Mutation	p.Ala10Thr(p.A10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676621:25676621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945G>A
AA Mutation	p.Glu649Lys(p.E649K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676612:25676612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754178434
CDS Mutation	c.1936G>A
AA Mutation	p.Glu646Lys(p.E646K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676138:25676138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462G>T
AA Mutation	p.Ala488Ser(p.A488S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676202:25676202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526G>A
AA Mutation	p.Arg509His(p.R509H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25676239:25676239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25671648:25671648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25662554:25662554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145841234
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25676350:25676350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1674C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25674390:25674390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116034603
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000382051
Start	25676621:25676621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1945G>T
AA Mutation	p.Glu649Ter(p.E649*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC34A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676614:25676614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938G>T
AA Mutation	p.Glu646Asp(p.E646D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25676363:25676363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766256521
CDS Mutation	c.1687G>A
AA Mutation	p.Val563Ile(p.V563I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382051
Start	25662543:25662543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759231403
CDS Mutation	c.43G>A
AA Mutation	p.Asp15Asn(p.D15N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25664284:25664284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144239727
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25669710:25669710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116552692
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382051
Start	25676428:25676428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150425667
CDS Mutation	c.1752G>A
Mutation Classification	Silent
Feature Type	Transcript