Colon Cancer: Gene >> SLC23A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4869943:4869943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1213T>C
AA Mutation	p.Ser405Pro(p.S405P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4862004:4862004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1568C>T
AA Mutation	p.Ser523Leu(p.S523L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4862028:4862028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544G>T
AA Mutation	p.Arg515Leu(p.R515L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4912948:4912948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142322986
CDS Mutation	c.139G>A
AA Mutation	p.Gly47Ser(p.G47S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4885865:4885865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527C>T
AA Mutation	p.Ala176Val(p.A176V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4899631:4899631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>T
AA Mutation	p.Ala136Ser(p.A136S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4883712:4883712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754G>A
AA Mutation	p.Ala252Thr(p.A252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4899641:4899641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs578152528
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4899683:4899683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767276768
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4932479:4932479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4861988:4861988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369987109
CDS Mutation	c.1584C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4874081:4874081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4874636:4874636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4857137:4857137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766502033
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338244
Start	4862881:4862881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756072858
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338244
Start	4883814:4883814(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.652delG
AA Mutation	p.Ala218ProfsTer7(p.A218Pfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338244
Start	4857089:4857089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1836delA
AA Mutation	p.Lys612AsnfsTer64(p.K612Nfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000338244
Start	4902510:4902510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256C>T
AA Mutation	p.Arg86Ter(p.R86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000338244
Start	4859385:4859385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1625-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC23A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338244
Start	4869943:4869943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1213T>A
AA Mutation	p.Ser405Thr(p.S405T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338244
Start	4899603:4899603(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.434delT
AA Mutation	p.Phe145SerfsTer38(p.F145Sfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript