Colon Cancer: Gene >> BTN2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26468061:26468061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>A
AA Mutation	p.Pro366Thr(p.P366T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26468148:26468148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781067055
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Met(p.V395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26459591:26459591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Trp(p.R65W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26468176:26468176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211G>T
AA Mutation	p.Arg404Ile(p.R404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26459547:26459547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149G>T
AA Mutation	p.Arg50Leu(p.R50L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26459634:26459634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236A>C
AA Mutation	p.Lys79Thr(p.K79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26459813:26459813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415C>T
AA Mutation	p.His139Tyr(p.H139Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312541
Start	26465219:26465219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312541
Start	26468117:26468117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312541
Start	26463371:26463371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312541
Start	26468048:26468048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568266180
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312541
Start	26465296:26465296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762471828
CDS Mutation	c.830delA
AA Mutation	p.Lys277ArgfsTer18(p.K277Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000312541
Start	26465343:26465343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871G>T
AA Mutation	p.Glu291Ter(p.E291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312541
Start	26465295:26465296(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.830dupA
AA Mutation	p.Ile278AspfsTer9(p.I278Dfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000312541
Start	26465974:26465974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145303049
CDS Mutation	c.955+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> BTN2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312541
Start	26468440:26468440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1475G>A
AA Mutation	p.Cys492Tyr(p.C492Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000312541
Start	26465343:26465343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871G>T
AA Mutation	p.Glu291Ter(p.E291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript