Colon Cancer: Gene >> BTN2A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26388144:26388144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144410497
CDS Mutation	c.574G>A
AA Mutation	p.Ala192Thr(p.A192T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26390022:26390022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780217318
CDS Mutation	c.742G>A
AA Mutation	p.Ala248Thr(p.A248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26392392:26392392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>A
AA Mutation	p.Pro333Thr(p.P333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26392819:26392819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1424C>T
AA Mutation	p.Ala475Val(p.A475V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26385303:26385303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752299416
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26392792:26392792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397C>T
AA Mutation	p.Ser466Leu(p.S466L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26385081:26385081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26385254:26385254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775875965
CDS Mutation	c.334G>A
AA Mutation	p.Val112Met(p.V112M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26385147:26385147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>G
AA Mutation	p.Ser76Cys(p.S76C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26385100:26385100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>T
AA Mutation	p.Glu60Asp(p.E60D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356709
Start	26383830:26383830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356709
Start	26388176:26388176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752559720
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356709
Start	26392490:26392490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776923192
CDS Mutation	c.1095C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356709
Start	26385178:26385178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356709
Start	26392868:26392868(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1476delC
AA Mutation	p.Ile493SerfsTer20(p.I493Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356709
Start	26388076:26388086(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.507_517delCATATCTGGAG
AA Mutation	p.Cys169TrpfsTer16(p.C169Wfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BTN2A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26385080:26385080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370867259
CDS Mutation	c.160C>T
AA Mutation	p.Arg54Cys(p.R54C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356709
Start	26388269:26388269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>T
AA Mutation	p.Glu233Asp(p.E233D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356709
Start	26392871:26392871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1476C>T
Mutation Classification	Silent
Feature Type	Transcript