Colon Cancer: Gene >> SOAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179342118:179342118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749244142
CDS Mutation	c.785G>A
AA Mutation	p.Arg262His(p.R262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179341186:179341186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770466169
CDS Mutation	c.656G>A
AA Mutation	p.Arg219His(p.R219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179323445:179323445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>T
AA Mutation	p.Asp43Tyr(p.D43Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179341072:179341072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542T>G
AA Mutation	p.Phe181Cys(p.F181C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179353627:179353627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770741362
CDS Mutation	c.1639C>T
AA Mutation	p.Arg547Cys(p.R547C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179335605:179335605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277G>T
AA Mutation	p.Ala93Ser(p.A93S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367619
Start	179350361:179350361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754865971
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367619
Start	179351405:179351405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367619
Start	179351457:179351457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1595delA
AA Mutation	p.Asn532IlefsTer34(p.N532Ifs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000367619
Start	179339547:179339547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SOAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367619
Start	179342121:179342121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788T>G
AA Mutation	p.Phe263Cys(p.F263C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript