Colon Cancer: Gene >> SSBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371320
Start	54228460:54228460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>A
AA Mutation	p.Gly342Arg(p.G342R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371320
Start	54404633:54404633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Gln(p.R45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371320
Start	54228307:54228307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362Gln(p.R362Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371320
Start	54240908:54240908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371320
Start	54257170:54257170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368799292
CDS Mutation	c.464G>A
AA Mutation	p.Arg155Gln(p.R155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371320
Start	54243288:54243288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368053178
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371320
Start	54228300:54228300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151171870
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371320
Start	54228791:54228791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764534702
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371320
Start	54404621:54404621(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.146delA
AA Mutation	p.Asn49ThrfsTer95(p.N49Tfs*95)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SSBP3

No Mutation Annotation!