Colon Cancer: Gene >> SLC5A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31487335:31487335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590T>C
AA Mutation	p.Leu197Pro(p.L197P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31485783:31485783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358G>A
AA Mutation	p.Ala120Thr(p.A120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31488738:31488738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Cys(p.R416C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31490509:31490509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764033463
CDS Mutation	c.1993G>A
AA Mutation	p.Val665Met(p.V665M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31487537:31487537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.663C>G
AA Mutation	p.His221Gln(p.H221Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31488751:31488751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1259G>A
AA Mutation	p.Arg420His(p.R420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31490468:31490468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368071047
CDS Mutation	c.1952G>A
AA Mutation	p.Arg651His(p.R651H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31489297:31489297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754404838
CDS Mutation	c.1624C>T
AA Mutation	p.Leu542Phe(p.L542F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31485813:31485813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760532652
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Cys(p.R130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31486206:31486206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>A
AA Mutation	p.Ala169Thr(p.A169T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31488891:31488891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1292T>C
AA Mutation	p.Val431Ala(p.V431A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31489243:31489243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1570G>A
AA Mutation	p.Val524Met(p.V524M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000330498
Start	31489252:31489252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579C>A
AA Mutation	p.Leu527Ile(p.L527I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31485797:31485797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31489221:31489221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539749063
CDS Mutation	c.1548G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31488910:31488910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31488411:31488411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31490508:31490508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375802106
CDS Mutation	c.1992C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31489302:31489302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779189173
CDS Mutation	c.1629G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330498
Start	31483175:31483175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.43delG
AA Mutation	p.Ala15ProfsTer5(p.A15Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330498
Start	31487372:31487372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.632delG
AA Mutation	p.Gly211AlafsTer30(p.G211Afs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC5A2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330498
Start	31488393:31488393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330498
Start	31484827:31484830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.211_214delCTCT
AA Mutation	p.Leu71SerfsTer47(p.L71Sfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript