Colon Cancer: Gene >> SLC22A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160442766:160442766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294G>T
AA Mutation	p.Ala432Ser(p.A432S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160451043:160451043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1658G>A
AA Mutation	p.Arg553His(p.R553H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160398001:160398001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160410748:160410748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142228053
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Cys(p.R293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160410800:160410800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753918761
CDS Mutation	c.929G>A
AA Mutation	p.Arg310His(p.R310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160437085:160437085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189883656
CDS Mutation	c.1162G>A
AA Mutation	p.Val388Met(p.V388M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160437143:160437143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145082363
CDS Mutation	c.1220G>A
AA Mutation	p.Arg407His(p.R407H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275300
Start	160443660:160443660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275300
Start	160408772:160408772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573086930
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000275300
Start	160450995:160450995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1611-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160437041:160437041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1118G>T
AA Mutation	p.Gly373Val(p.G373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275300
Start	160443691:160443691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459C>A
AA Mutation	p.Leu487Met(p.L487M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript