Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PAPSS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107653571:107653571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107631707:107631707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1660A>G
AA Mutation	p.Thr554Ala(p.T554A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107614355:107614355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770488612
CDS Mutation	c.1769G>A
AA Mutation	p.Arg590Gln(p.R590Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107644924:107644924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384G>A
AA Mutation	p.Asp462Asn(p.D462N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107631735:107631735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1632A>C
AA Mutation	p.Lys544Asn(p.K544N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107693907:107693907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763373160
CDS Mutation	c.275G>A
AA Mutation	p.Arg92His(p.R92H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265174
Start	107720165:107720165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PAPSS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107693842:107693842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11555779
CDS Mutation	c.340G>A
AA Mutation	p.Ala114Thr(p.A114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265174
Start	107693892:107693892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290A>C
AA Mutation	p.Lys97Thr(p.K97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265174
Start	107687133:107687133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137920897
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript