Colon Cancer: Gene >> SLC25A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281456
Start	185144996:185144996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>A
AA Mutation	p.Gly115Asp(p.G115D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281456
Start	185145817:185145817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657T>G
AA Mutation	p.Ser219Arg(p.S219R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281456
Start	185145107:185145107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>A
AA Mutation	p.Arg152His(p.R152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000281456
Start	185146814:185146814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281456
Start	185146922:185146922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848G>A
AA Mutation	p.Gly283Asp(p.G283D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281456
Start	185146923:185146923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374918344
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000281456
Start	185145039:185145039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.387C>A
AA Mutation	p.Cys129Ter(p.C129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A4

No Mutation Annotation!