Colon Cancer: Gene >> SLC23A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139372089:139372089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714T>C
AA Mutation	p.Ser572Pro(p.S572P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139378649:139378649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109C>T
AA Mutation	p.Ala370Val(p.A370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139380587:139380587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443T>C
AA Mutation	p.Ile148Thr(p.I148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139381977:139381977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376047353
CDS Mutation	c.223G>A
AA Mutation	p.Asp75Asn(p.D75N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139372023:139372023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780G>A
AA Mutation	p.Val594Met(p.V594M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139377464:139377464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1487T>A
AA Mutation	p.Leu496Gln(p.L496Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139378044:139378044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769262149
CDS Mutation	c.1384G>A
AA Mutation	p.Gly462Arg(p.G462R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139379697:139379697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906G>T
AA Mutation	p.Trp302Cys(p.W302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139378026:139378026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1402G>A
AA Mutation	p.Gly468Arg(p.G468R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139378030:139378030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1398C>A
AA Mutation	p.Phe466Leu(p.F466L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139380358:139380358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497T>C
AA Mutation	p.Val166Ala(p.V166A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139381932:139381932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774361660
CDS Mutation	c.268G>A
AA Mutation	p.Val90Met(p.V90M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139379770:139379770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>T
AA Mutation	p.Pro278Leu(p.P278L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139382555:139382555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87T>G
AA Mutation	p.Phe29Leu(p.F29L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139380290:139380290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565A>G
AA Mutation	p.Thr189Ala(p.T189A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139372036:139372036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1767A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139379959:139379959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139377439:139377439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139378105:139378105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1323T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139372111:139372111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC23A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139372076:139372076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1727A>C
AA Mutation	p.Lys576Thr(p.K576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348729
Start	139382536:139382536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753453829
CDS Mutation	c.106G>A
AA Mutation	p.Glu36Lys(p.E36K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139379233:139379233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348729
Start	139382582:139382582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770164957
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript