Colon Cancer: Gene >> SLC18A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611000:49611000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260C>T
AA Mutation	p.Pro87Leu(p.P87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49612133:49612133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1393G>A
AA Mutation	p.Val465Ile(p.V465I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49612244:49612244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504C>T
AA Mutation	p.Arg502Cys(p.R502C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49612275:49612275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1535G>A
AA Mutation	p.Arg512His(p.R512H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611971:49611971(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	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611975:49611975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766544544
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611012:49611012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272G>A
AA Mutation	p.Ser91Asn(p.S91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611507:49611507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767C>T
AA Mutation	p.Ala256Val(p.A256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49610799:49610799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59C>A
AA Mutation	p.Ala20Asp(p.A20D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611681:49611681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Met(p.T314M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611998:49611998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258G>A
AA Mutation	p.Val420Ile(p.V420I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611351:49611351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611A>G
AA Mutation	p.Tyr204Cys(p.Y204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49612026:49612026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286C>T
AA Mutation	p.Ser429Leu(p.S429L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49610900:49610900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Val54Met(p.V54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611656:49611656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.916G>A
AA Mutation	p.Ala306Thr(p.A306T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611506:49611506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766G>A
AA Mutation	p.Ala256Thr(p.A256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611668:49611668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928C>T
AA Mutation	p.Pro310Ser(p.P310S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611842:49611842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102G>A
AA Mutation	p.Gly368Ser(p.G368S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611625:49611625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611880:49611880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49610860:49610860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611196:49611196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611739:49611739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611313:49611313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49610794:49610794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49610854:49610854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611277:49611277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC18A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611086:49611086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>A
AA Mutation	p.Pro116Thr(p.P116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611033:49611033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293C>T
AA Mutation	p.Ser98Leu(p.S98L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374115
Start	49611665:49611665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925G>A
AA Mutation	p.Glu309Lys(p.E309K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374115
Start	49611202:49611202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript