Colon Cancer: Gene >> SGK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000237305
Start	134171091:134171091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772324787
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000237305
Start	134172762:134172762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562C>A
AA Mutation	p.Leu188Ile(p.L188I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367858
Start	134261956:134261956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262T>G
AA Mutation	p.Trp88Gly(p.W88G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367858
Start	134317425:134317425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36G>T
AA Mutation	p.Lys12Asn(p.K12N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237305
Start	134170346:134170346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772508033
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000237305
Start	134170916:134170916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SGK1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000237305
Start	134170895:134170895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1059C>A
Mutation Classification	Silent
Feature Type	Transcript