Colon Cancer: Gene >> FOXP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318789
Start	70976955:70976955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759521321
CDS Mutation	c.1516G>A
AA Mutation	p.Ala506Thr(p.A506T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318789
Start	70977833:70977833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763413735
CDS Mutation	c.1343C>T
AA Mutation	p.Ser448Leu(p.S448L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318789
Start	71198276:71198276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Trp(p.R36W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318789
Start	71198260:71198260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756099573
CDS Mutation	c.122C>T
AA Mutation	p.Thr41Met(p.T41M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000318789
Start	70966056:70966056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1723G>T
AA Mutation	p.Ala575Ser(p.A575S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318789
Start	70972666:70972666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs797045586
CDS Mutation	c.1541G>A
AA Mutation	p.Arg514His(p.R514H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318789
Start	70977684:70977684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387G>A
AA Mutation	p.Glu463Lys(p.E463K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318789
Start	71015599:71015599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318789
Start	70977832:70977832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143503790
CDS Mutation	c.1344G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318789
Start	71198295:71198295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550457312
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318789
Start	70977936:70977936(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs797044652
CDS Mutation	c.1240delC
AA Mutation	p.Leu414Ter(p.L414*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000318789
Start	71001004:71001004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Gln344Ter(p.Q344*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000318789
Start	71052617:71052617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430C>T
AA Mutation	p.Gln144Ter(p.Q144*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXP1

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318789
Start	71052549:71052550(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.497_498delAA
AA Mutation	p.Lys166ThrfsTer3(p.K166Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript