Colon Cancer: Gene >> SLC25A22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320230
Start	792427:792427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753519140
CDS Mutation	c.619C>T
AA Mutation	p.Leu207Phe(p.L207F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320230
Start	794786:794786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136T>A
AA Mutation	p.Tyr46Asn(p.Y46N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320230
Start	794885:794885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37A>G
AA Mutation	p.Ile13Val(p.I13V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320230
Start	794874:794874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320230
Start	792332:792332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762903578
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320230
Start	792633:792633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540297776
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320230
Start	793588:793588(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.234delC
AA Mutation	p.Glu79ArgfsTer23(p.E79Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A22

No Mutation Annotation!