Colon Cancer: Gene >> RANBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5941684:5941684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343T>C
AA Mutation	p.Tyr115His(p.Y115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5923280:5923280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749250391
CDS Mutation	c.1123G>A
AA Mutation	p.Ala375Thr(p.A375T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5951475:5951475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200C>T
AA Mutation	p.Ala67Val(p.A67V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5917626:5917626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688C>T
AA Mutation	p.Thr563Met(p.T563M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000340578
Start	5951394:5951394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>A
AA Mutation	p.Gly94Glu(p.G94E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5951404:5951404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Glu91Lys(p.E91K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5918633:5918633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1336C>T
AA Mutation	p.Arg446Trp(p.R446W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5923300:5923300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103C>T
AA Mutation	p.Ser368Phe(p.S368F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340578
Start	5917843:5917843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191712763
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340578
Start	5951546:5951546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340578
Start	5928025:5928025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.756delA
AA Mutation	p.Asp253ThrfsTer14(p.D253Tfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RANBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340578
Start	5918549:5918549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Cys(p.R474C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript