Colon Cancer: Gene >> IGF2BP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23347699:23347699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719C>A
AA Mutation	p.Ala240Asp(p.A240D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23342083:23342083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184C>T
AA Mutation	p.Pro395Leu(p.P395L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23312747:23312747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1629C>A
AA Mutation	p.Phe543Leu(p.F543L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23351316:23351316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672G>T
AA Mutation	p.Gln224His(p.Q224H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23317677:23317677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357A>C
AA Mutation	p.Met453Leu(p.M453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23345981:23345981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900A>C
AA Mutation	p.Lys300Asn(p.K300N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23468534:23468534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Glu62Lys(p.E62K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23351510:23351510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145484983
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258729
Start	23319165:23319165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258729
Start	23342130:23342130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000258729
Start	23468534:23468534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184G>T
AA Mutation	p.Glu62Ter(p.E62*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000258729
Start	23351483:23351483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Ter(p.R169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IGF2BP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23346041:23346041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840G>T
AA Mutation	p.Lys280Asn(p.K280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258729
Start	23347708:23347708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202212306
CDS Mutation	c.710C>T
AA Mutation	p.Ala237Val(p.A237V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript