Colon Cancer: Gene >> IGF2BP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49038361:49038361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Trp(p.R199W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49042342:49042342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Trp(p.R348W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49031913:49031913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341A>G
AA Mutation	p.Asn114Ser(p.N114S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49046345:49046345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613A>T
AA Mutation	p.Lys538Ile(p.K538I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49038422:49038422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656G>A
AA Mutation	p.Arg219His(p.R219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49046282:49046282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550C>T
AA Mutation	p.Thr517Met(p.T517M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49046303:49046303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571C>T
AA Mutation	p.Pro524Leu(p.P524L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49045983:49045983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489T>G
AA Mutation	p.Ser497Ala(p.S497A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49046001:49046001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507A>G
AA Mutation	p.Ile503Val(p.I503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49042302:49042302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002G>T
AA Mutation	p.Glu334Asp(p.E334D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49025638:49025638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257G>A
AA Mutation	p.Arg86Gln(p.R86Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49038286:49038286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779507141
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Trp(p.R174W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49042300:49042300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752711229
CDS Mutation	c.1000G>A
AA Mutation	p.Glu334Lys(p.E334K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290341
Start	49045047:49045047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754609010
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290341
Start	49038321:49038321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774524369
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290341
Start	48997829:48997829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290341
Start	49042299:49042299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290341
Start	49042290:49042290(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.994delG
AA Mutation	p.Ala332ProfsTer12(p.A332Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290341
Start	49039995:49039995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.726delA
AA Mutation	p.Ala243ProfsTer17(p.A243Pfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000290341
Start	49040072:49040072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>T
AA Mutation	p.Glu267Ter(p.E267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000290341
Start	49038268:49038268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Ter(p.R168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IGF2BP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49038287:49038287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746549698
CDS Mutation	c.521G>A
AA Mutation	p.Arg174Gln(p.R174Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49040039:49040039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777305494
CDS Mutation	c.766G>A
AA Mutation	p.Ala256Thr(p.A256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49038201:49038201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435G>T
AA Mutation	p.Glu145Asp(p.E145D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49039982:49039982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375360274
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290341
Start	49042300:49042300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752711229
CDS Mutation	c.1000G>A
AA Mutation	p.Glu334Lys(p.E334K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript