Colon Cancer: Gene >> TMEM50A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374358
Start	25340544:25340544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>T
AA Mutation	p.Arg20Cys(p.R20C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374358
Start	25351681:25351681(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	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374358
Start	25340539:25340539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756708288
CDS Mutation	c.53A>G
AA Mutation	p.Glu18Gly(p.E18G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374358
Start	25342991:25342991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374358
Start	25352901:25352901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573180713
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM50A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374358
Start	25356798:25356798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373G>T
AA Mutation	p.Asp125Tyr(p.D125Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374358
Start	25340507:25340507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21C>A
Mutation Classification	Silent
Feature Type	Transcript