Product Details
- SNP ID
-
rs80075458
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:87935077 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AAGAGGAAGGAAAACCGCTTCGTGG[A/T]GCGCCAGAGCATCGTGCCACTGCGC
- Phenotype
-
MIM: 603709
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ADAM22
PubMed Links
Gene Details
- Gene
- ADAM22
- Gene Name
- ADAM metallopeptidase domain 22
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001324417.1 |
352 |
Missense Mutation |
GAG,GTG |
E45V |
NP_001311346.1 |
NM_001324418.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_001311347.1 |
NM_001324419.1 |
352 |
Missense Mutation |
GAG,GTG |
E45V |
NP_001311348.1 |
NM_001324420.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_001311349.1 |
NM_001324421.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_001311350.1 |
NM_004194.4 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_004185.1 |
NM_016351.5 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_057435.2 |
NM_021721.4 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_068367.1 |
NM_021722.5 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_068368.2 |
NM_021723.4 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
NP_068369.1 |
XM_005250445.3 |
352 |
Missense Mutation |
GAG,GTG |
E98V |
XP_005250502.1 |
XM_006716028.3 |
352 |
Missense Mutation |
GAG,GTG |
E98V |
XP_006716091.1 |
XM_006716029.3 |
352 |
Missense Mutation |
GAG,GTG |
E98V |
XP_006716092.1 |
XM_011516318.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_011514620.1 |
XM_011516319.2 |
352 |
Missense Mutation |
GAG,GTG |
E45V |
XP_011514621.1 |
XM_011516320.2 |
352 |
Missense Mutation |
GAG,GTG |
E98V |
XP_011514622.1 |
XM_011516321.2 |
352 |
Missense Mutation |
GAG,GTG |
E98V |
XP_011514623.1 |
XM_011516322.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_011514624.1 |
XM_011516323.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_011514625.1 |
XM_011516324.1 |
352 |
Intron |
|
|
XP_011514626.1 |
XM_017012329.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867818.1 |
XM_017012330.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867819.1 |
XM_017012331.1 |
352 |
Missense Mutation |
GAG,GTG |
E45V |
XP_016867820.1 |
XM_017012332.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867821.1 |
XM_017012333.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867822.1 |
XM_017012334.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867823.1 |
XM_017012335.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867824.1 |
XM_017012336.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867825.1 |
XM_017012337.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867826.1 |
XM_017012338.1 |
352 |
Missense Mutation |
GAG,GTG |
E45V |
XP_016867827.1 |
XM_017012339.1 |
352 |
Missense Mutation |
GAG,GTG |
E46V |
XP_016867828.1 |
XM_017012340.1 |
352 |
Intron |
|
|
XP_016867829.1 |
XM_017012341.1 |
352 |
UTR 5 |
|
|
XP_016867830.1 |
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