Colon Cancer: Gene >> SLC44A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10632094:10632094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749777162
CDS Mutation	c.761G>A
AA Mutation	p.Arg254His(p.R254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10636495:10636495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406C>T
AA Mutation	p.Ala469Val(p.A469V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335757
Start	10631533:10631533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500C>A
AA Mutation	p.Pro167His(p.P167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10631347:10631347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403T>C
AA Mutation	p.Tyr135His(p.Y135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10634855:10634855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923A>G
AA Mutation	p.Tyr308Cys(p.Y308C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10636534:10636534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445C>T
AA Mutation	p.Pro482Leu(p.P482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10626256:10626256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41C>T
AA Mutation	p.Thr14Met(p.T14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335757
Start	10642368:10642368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764490981
CDS Mutation	c.1931C>T
AA Mutation	p.Thr644Met(p.T644M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335757
Start	10638041:10638041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335757
Start	10631901:10631901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148167135
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335757
Start	10637888:10637888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1728G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335757
Start	10635199:10635199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335757
Start	10632053:10632053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335757
Start	10635218:10635218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335757
Start	10631718:10631718(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.599delA
AA Mutation	p.Asn200ThrfsTer16(p.N200Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC44A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335757
Start	10636732:10636732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1567G>A
AA Mutation	p.Glu523Lys(p.E523K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript