Colon Cancer: Gene >> TMEM259

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356663
Start	1011128:1011128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285C>A
AA Mutation	p.Leu429Met(p.L429M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356663
Start	1010562:1010562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771672096
CDS Mutation	c.1651G>A
AA Mutation	p.Ala551Thr(p.A551T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356663
Start	1014338:1014338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750855238
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Cys(p.R121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356663
Start	1020787:1020787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210C>A
AA Mutation	p.Phe70Leu(p.F70L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356663
Start	1013276:1013276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572G>A
AA Mutation	p.Ser191Asn(p.S191N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356663
Start	1012512:1012512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772542168
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356663
Start	1010635:1010635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762153382
CDS Mutation	c.1578G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356663
Start	1014297:1014297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774357446
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000356663
Start	1011159:1011159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254T>A
AA Mutation	p.Tyr418Ter(p.Y418*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM259

No Mutation Annotation!