Product Details
- SNP ID
-
rs144315631
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:49815073 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCCACACCACCCTGGTTGTCACGA[C/T]GAAACTGGTGCTCCCGACCCCTGGC
- Phenotype
-
MIM: 612730
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SLC9A8
PubMed Links
Gene Details
- Gene
- SLC9A8
- Gene Name
- solute carrier family 9 member A8
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001260491.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
NP_001247420.1 |
NM_015266.2 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
NP_056081.1 |
XM_006723756.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_006723819.1 |
XM_011528736.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527038.1 |
XM_011528737.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527039.1 |
XM_011528738.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527040.1 |
XM_011528739.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527041.1 |
XM_011528740.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527042.1 |
XM_011528741.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527043.1 |
XM_011528742.1 |
164 |
UTR 5 |
|
|
XP_011527044.1 |
XM_011528743.2 |
164 |
Intron |
|
|
XP_011527045.1 |
XM_011528744.2 |
164 |
Intron |
|
|
XP_011527046.1 |
XM_011528745.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_011527047.1 |
XM_017027754.1 |
164 |
Missense Mutation |
ACG,ATG |
T31M |
XP_016883243.1 |
XM_017027755.1 |
164 |
UTR 5 |
|
|
XP_016883244.1 |
XM_017027756.1 |
164 |
UTR 5 |
|
|
XP_016883245.1 |
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