Colon Cancer: Gene >> TOMM34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372813
Start	44943142:44943142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897G>T
AA Mutation	p.Lys299Asn(p.K299N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372813
Start	44951961:44951961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756307089
CDS Mutation	c.422G>T
AA Mutation	p.Arg141Leu(p.R141L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372813
Start	44955186:44955186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>A
AA Mutation	p.Leu88Met(p.L88M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372813
Start	44951891:44951891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492G>T
AA Mutation	p.Glu164Asp(p.E164D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TOMM34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372813
Start	44951895:44951895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488C>T
AA Mutation	p.Ser163Leu(p.S163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372813
Start	44955085:44955085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363C>A
Mutation Classification	Silent
Feature Type	Transcript