Colon Cancer: Gene >> HNRNPCL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12847791:12847791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377179680
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Trp(p.R167W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12847568:12847568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722A>G
AA Mutation	p.Glu241Gly(p.E241G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12848159:12848159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772611920
CDS Mutation	c.131C>T
AA Mutation	p.Ala44Val(p.A44V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12847856:12847856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4026148
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12847803:12847803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148638726
CDS Mutation	c.487A>G
AA Mutation	p.Lys163Glu(p.K163E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12847703:12847703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752818797
CDS Mutation	c.587C>A
AA Mutation	p.Ser196Tyr(p.S196Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317869
Start	12847862:12847862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189811978
CDS Mutation	c.428C>T
AA Mutation	p.Ser143Leu(p.S143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317869
Start	12848260:12848260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317869
Start	12848008:12848008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763260718
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317869
Start	12848143:12848143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000317869
Start	12847542:12847542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748G>T
AA Mutation	p.Glu250Ter(p.E250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPCL1

No Mutation Annotation!