Colon Cancer: Gene >> SLC39A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356736
Start	102305059:102305059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605T>C
AA Mutation	p.Val202Ala(p.V202A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356736
Start	102307599:102307599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389G>A
AA Mutation	p.Gly130Glu(p.G130E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356736
Start	102305104:102305104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560G>T
AA Mutation	p.Gly187Val(p.G187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356736
Start	102344584:102344584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356736
Start	102267990:102267990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371697716
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356736
Start	102268068:102268068(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.852delA
AA Mutation	p.Glu285SerfsTer8(p.E285Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000356736
Start	102263061:102263061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1366G>T
AA Mutation	p.Glu456Ter(p.E456*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A8

No Mutation Annotation!