Colon Cancer: Gene >> BTNL9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181047993:181047993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176G>A
AA Mutation	p.Cys59Tyr(p.C59Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181059696:181059696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369125172
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181047984:181047984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167A>G
AA Mutation	p.Glu56Gly(p.E56G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181050225:181050225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758793047
CDS Mutation	c.592T>C
AA Mutation	p.Phe198Leu(p.F198L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181059569:181059569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>A
AA Mutation	p.Ala439Thr(p.A439T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181048158:181048158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341G>T
AA Mutation	p.Gly114Val(p.G114V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327705
Start	181045524:181045524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35A>T
AA Mutation	p.Lys12Met(p.K12M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327705
Start	181059652:181059652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327705
Start	181047991:181047991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138816460
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327705
Start	181048150:181048150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112433732
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327705
Start	181059559:181059559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BTNL9

No Mutation Annotation!