Colon Cancer: Gene >> NDUFS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47582138:47582138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747054142
CDS Mutation	c.432G>C
AA Mutation	p.Lys144Asn(p.K144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47584339:47584339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78121716
CDS Mutation	c.653G>A
AA Mutation	p.Arg218Gln(p.R218Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47580866:47580866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263T>A
AA Mutation	p.Ile88Asn(p.I88N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47580605:47580605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214T>C
AA Mutation	p.Tyr72His(p.Y72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47582130:47582130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146407178
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47579125:47579125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201457989
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Cys(p.R12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263774
Start	47579102:47579102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11C>T
AA Mutation	p.Ala4Val(p.A4V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263774
Start	47582195:47582195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NDUFS3

No Mutation Annotation!