Colon Cancer: Gene >> BTNL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342868
Start	181005469:181005469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>A
AA Mutation	p.Ser333Tyr(p.S333Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342868
Start	180993049:180993049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771112486
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342868
Start	181005791:181005791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342868
Start	181004758:181004758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371454208
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342868
Start	181005665:181005665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1200delC
AA Mutation	p.Ser401AlafsTer7(p.S401Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342868
Start	180997295:180997295(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.484delC
AA Mutation	p.Gln162SerfsTer35(p.Q162Sfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342868
Start	180993152:180993152(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.391delG
AA Mutation	p.Val131TrpfsTer66(p.V131Wfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342868
Start	180993043:180993043(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.285delG
AA Mutation	p.Arg96ValfsTer4(p.R96Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BTNL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342868
Start	181005406:181005406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>T
AA Mutation	p.Arg312Ile(p.R312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342868
Start	181005665:181005665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1200delC
AA Mutation	p.Ser401AlafsTer7(p.S401Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript