Colon Cancer: Gene >> SAMD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368134
Start	130144549:130144549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371432532
CDS Mutation	c.1534G>A
AA Mutation	p.Glu512Lys(p.E512K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368134
Start	130154826:130154826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022A>G
AA Mutation	p.Gln341Arg(p.Q341R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368134
Start	130146174:130146174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1031G>A
AA Mutation	p.Arg344Lys(p.R344K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368134
Start	130154867:130154867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>T
AA Mutation	p.Lys327Asn(p.K327N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368134
Start	130214423:130214423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183A>C
AA Mutation	p.Lys61Asn(p.K61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368134
Start	130184160:130184160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768298745
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368134
Start	130146120:130146120(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1085delT
AA Mutation	p.Leu362TrpfsTer9(p.L362Wfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368134
Start	130214420:130214420(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770241311
CDS Mutation	c.186delA
AA Mutation	p.Lys62AsnfsTer9(p.K62Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368134
Start	130145358:130145358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1260delT
AA Mutation	p.Phe420LeufsTer4(p.F420Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000368134
Start	130175966:130175966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Ter(p.R233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SAMD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368134
Start	130144584:130144584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1499G>T
AA Mutation	p.Ser500Ile(p.S500I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368134
Start	130214366:130214366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.240C>A
Mutation Classification	Silent
Feature Type	Transcript