Colon Cancer: Gene >> SLC43A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301335
Start	1613215:1613215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481A>T
AA Mutation	p.Met161Leu(p.M161L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301335
Start	1627847:1627847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28C>T
AA Mutation	p.Arg10Trp(p.R10W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301335
Start	1583308:1583308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Trp(p.R416W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301335
Start	1591639:1591639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Gly219Arg(p.G219R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301335
Start	1613263:1613263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201908715
CDS Mutation	c.433G>A
AA Mutation	p.Val145Met(p.V145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301335
Start	1615023:1615023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200135342
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301335
Start	1616726:1616726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301335
Start	1627752:1627752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000301335
Start	1576595:1576595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1548+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC43A2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301335
Start	1578276:1578276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372871741
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript