Product Details
- SNP ID
-
rs141799611
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:24300076 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGAGAGGCCAAAGAGCCAGAGCAAC[A/G]GGTACAGCTTTTGATTTATCAAAGG
- Phenotype
-
MIM: 606188
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ADAM28
PubMed Links
Gene Details
- Gene
- ADAM28
- Gene Name
- ADAM metallopeptidase domain 28
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001304351.1 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
NP_001291280.1 |
NM_014265.5 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
NP_055080.2 |
NM_021777.4 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
NP_068547.2 |
XM_005273380.3 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_005273437.1 |
XM_005273382.1 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_005273439.1 |
XM_006716273.3 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_006716336.1 |
XM_006716274.1 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_006716337.1 |
XM_011544367.2 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_011542669.1 |
XM_011544368.2 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_011542670.1 |
XM_011544369.2 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_011542671.1 |
XM_011544370.2 |
259 |
UTR 5 |
|
|
XP_011542672.1 |
XM_011544371.2 |
259 |
Intron |
|
|
XP_011542673.1 |
XM_017012974.1 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_016868463.1 |
XM_017012975.1 |
259 |
Missense Mutation |
CAG,CGG |
Q50R |
XP_016868464.1 |
XM_017012976.1 |
259 |
UTR 5 |
|
|
XP_016868465.1 |
- Gene
- LOC101929294
- Gene Name
- uncharacterized LOC101929294
There are no transcripts associated with this gene.
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