Colon Cancer: Gene >> BTN3A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26451734:26451734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149504053
CDS Mutation	c.1078A>G
AA Mutation	p.Arg360Gly(p.R360G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26443629:26443629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55T>C
AA Mutation	p.Phe19Leu(p.F19L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26451707:26451707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574858167
CDS Mutation	c.1051G>A
AA Mutation	p.Ala351Thr(p.A351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26445967:26445967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697G>A
AA Mutation	p.Ala233Thr(p.A233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26445811:26445811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541G>A
AA Mutation	p.Asp181Asn(p.D181N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26452134:26452134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1478A>G
AA Mutation	p.Glu493Gly(p.E493G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000244519
Start	26445786:26445786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.520delC
AA Mutation	p.Gln174AsnfsTer4(p.Q174Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BTN3A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26452392:26452392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144256388
CDS Mutation	c.1736G>A
AA Mutation	p.Arg579His(p.R579H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244519
Start	26444274:26444274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746463161
CDS Mutation	c.403G>A
AA Mutation	p.Glu135Lys(p.E135K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244519
Start	26445810:26445810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765497042
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript