Colon Cancer: Gene >> RNF34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121423395:121423395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369744966
CDS Mutation	c.938G>A
AA Mutation	p.Arg313Gln(p.R313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121423512:121423512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61754471
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352His(p.R352H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121417510:121417510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232T>A
AA Mutation	p.Cys78Ser(p.C78S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121417613:121417613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121417808:121417808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41507449
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361234
Start	121420283:121420283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190921881
CDS Mutation	c.675T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361234
Start	121420286:121420286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202132357
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RNF34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121417697:121417697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419A>T
AA Mutation	p.Lys140Ile(p.K140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121417873:121417873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595G>A
AA Mutation	p.Asp199Asn(p.D199N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361234
Start	121423505:121423505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>A
AA Mutation	p.Gly350Ser(p.G350S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361234
Start	121417533:121417533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255T>C
Mutation Classification	Silent
Feature Type	Transcript