Colon Cancer: Gene >> TMEM30A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230461
Start	75256268:75256268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778890689
CDS Mutation	c.920G>A
AA Mutation	p.Arg307Gln(p.R307Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230461
Start	75284439:75284439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200G>A
AA Mutation	p.Gly67Asp(p.G67D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230461
Start	75258903:75258903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769T>G
AA Mutation	p.Phe257Val(p.F257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000230461
Start	75259356:75259356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772644735
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Ter(p.R226*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000230461
Start	75265272:75265272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377408806
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Ter(p.R138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM30A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230461
Start	75256250:75256250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938G>A
AA Mutation	p.Ser313Asn(p.S313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230461
Start	75260908:75260908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457C>T
AA Mutation	p.Pro153Ser(p.P153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript