Product Details
- SNP ID
-
rs199667250
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:1483412 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCAGCGAGCGGATGGAGTTGTGGAG[A/G]CCGGCGCAGGCCGATACGTTTTCCC
- Phenotype
-
MIM: 600487
MIM: 609346
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C19orf25
PubMed Links
Gene Details
- Gene
- C19orf25
- Gene Name
- chromosome 19 open reading frame 25
There are no transcripts associated with this gene.
- Gene
- PCSK4
- Gene Name
- proprotein convertase subtilisin/kexin type 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_017573.4 |
1107 |
Silent Mutation |
GGC,GGT |
G481G |
NP_060043.2 |
XM_005259586.1 |
1107 |
Silent Mutation |
GGC,GGT |
G293G |
XP_005259643.1 |
XM_011528085.2 |
1107 |
Silent Mutation |
GGC,GGT |
G508G |
XP_011526387.1 |
XM_011528086.2 |
1107 |
Silent Mutation |
GGC,GGT |
G499G |
XP_011526388.1 |
XM_011528087.2 |
1107 |
Silent Mutation |
GGC,GGT |
G508G |
XP_011526389.1 |
XM_011528088.2 |
1107 |
Silent Mutation |
GGC,GGT |
G446G |
XP_011526390.1 |
XM_011528089.2 |
1107 |
Silent Mutation |
GGC,GGT |
G414G |
XP_011526391.1 |
XM_011528090.2 |
1107 |
Silent Mutation |
GGC,GGT |
G387G |
XP_011526392.1 |
XM_011528091.2 |
1107 |
Silent Mutation |
GGC,GGT |
G384G |
XP_011526393.1 |
XM_011528092.2 |
1107 |
Silent Mutation |
GGC,GGT |
G508G |
XP_011526394.1 |
XM_011528093.2 |
1107 |
Silent Mutation |
GGC,GGT |
G508G |
XP_011526395.1 |
XM_011528094.1 |
1107 |
Silent Mutation |
GGC,GGT |
G293G |
XP_011526396.1 |
XM_011528095.2 |
1107 |
Missense Mutation |
CCT,TCT |
P479S |
XP_011526397.1 |
XM_011528096.1 |
1107 |
Silent Mutation |
GGC,GGT |
G259G |
XP_011526398.1 |
XM_017026897.1 |
1107 |
Silent Mutation |
GGC,GGT |
G293G |
XP_016882386.1 |
- Gene
- REEP6
- Gene Name
- receptor accessory protein 6
There are no transcripts associated with this gene.
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