Colon Cancer: Gene >> SLC28A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84290161:84290161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142C>A
AA Mutation	p.Ser381Tyr(p.S381Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84285458:84285458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1534G>T
AA Mutation	p.Gly512Cys(p.G512C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84288132:84288132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761250487
CDS Mutation	c.1196C>T
AA Mutation	p.Ala399Val(p.A399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84302368:84302368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75061381
CDS Mutation	c.356C>T
AA Mutation	p.Ser119Leu(p.S119L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84280050:84280050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753167663
CDS Mutation	c.1753C>T
AA Mutation	p.Arg585Cys(p.R585C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84278231:84278231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2063C>G
AA Mutation	p.Ser688Cys(p.S688C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376238
Start	84292747:84292747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944T>A
AA Mutation	p.Val315Asp(p.V315D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376238
Start	84278302:84278302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756994145
CDS Mutation	c.1992C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376238
Start	84290172:84290172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774589116
CDS Mutation	c.1131T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376238
Start	84299701:84299701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376238
Start	84285366:84285366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147965649
CDS Mutation	c.1626C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376238
Start	84285511:84285512(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1480dupT
AA Mutation	p.Ser494PhefsTer21(p.S494Ffs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC28A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84290219:84290219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769712186
CDS Mutation	c.1084G>A
AA Mutation	p.Ala362Thr(p.A362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84305260:84305260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328T>G
AA Mutation	p.Leu110Val(p.L110V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376238
Start	84299650:84299650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600G>C
AA Mutation	p.Gln200His(p.Q200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376238
Start	84288101:84288101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770152872
CDS Mutation	c.1227T>C
Mutation Classification	Silent
Feature Type	Transcript