Colon Cancer: Gene >> SLMAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57831435:57831435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>T
AA Mutation	p.Arg84Ile(p.R84I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57757758:57757758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107G>A
AA Mutation	p.Arg36His(p.R36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57858118:57858118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367733735
CDS Mutation	c.646C>T
AA Mutation	p.Arg216Trp(p.R216W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57917062:57917062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2244G>T
AA Mutation	p.Lys748Asn(p.K748N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57912599:57912599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1867G>A
AA Mutation	p.Ala623Thr(p.A623T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57912454:57912454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1722A>C
AA Mutation	p.Arg574Ser(p.R574S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57831476:57831476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>A
AA Mutation	p.Leu98Ile(p.L98I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428312
Start	57831439:57831439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428312
Start	57757819:57757819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000428312
Start	57909105:57909105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603C>T
AA Mutation	p.Arg535Ter(p.R535*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLMAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000428312
Start	57864551:57864551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000428312
Start	57912403:57912403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79652350
CDS Mutation	c.1671C>T
Mutation Classification	Silent
Feature Type	Transcript