Colon Cancer: Gene >> ESRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94678259:94678259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708G>A
AA Mutation	p.Ala570Thr(p.A570T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94696855:94696855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1975G>A
AA Mutation	p.Ala659Thr(p.A659T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94665004:94665004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833A>G
AA Mutation	p.His278Arg(p.H278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94671570:94671570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351G>A
AA Mutation	p.Gly451Ser(p.G451S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433389
Start	94671454:94671454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235T>C
AA Mutation	p.Val412Ala(p.V412A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94665039:94665039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868A>T
AA Mutation	p.Met290Leu(p.M290L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94668174:94668174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157C>T
AA Mutation	p.Ala386Val(p.A386V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94696861:94696861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775408778
CDS Mutation	c.1981G>A
AA Mutation	p.Glu661Lys(p.E661K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000433389
Start	94674471:94674471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757908275
CDS Mutation	c.1616G>A
AA Mutation	p.Arg539Gln(p.R539Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433389
Start	94662276:94662276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433389
Start	94671539:94671539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1320T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433389
Start	94692731:94692731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369829287
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433389
Start	94674383:94674383(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775950025
CDS Mutation	c.1535delA
AA Mutation	p.Asn512ThrfsTer2(p.N512Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433389
Start	94674383:94674384(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1534_1535delAA
AA Mutation	p.Asn512HisfsTer7(p.N512Hfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433389
Start	94668009:94668009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.996delG
AA Mutation	p.Leu333SerfsTer55(p.L333Sfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433389
Start	94674382:94674383(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1535dupA
AA Mutation	p.Asn512LysfsTer8(p.N512Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000433389
Start	94674307:94674307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ESRP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433389
Start	94692731:94692731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369829287
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000433389
Start	94646216:94646216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>T
AA Mutation	p.Glu142Ter(p.E142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000433389
Start	94643324:94643324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>T
AA Mutation	p.Glu95Ter(p.E95*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript