Product Details
- SNP ID
-
rs149773783
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:190659567 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCTCATTTAAAAATCCCCAAATGT[C/G]CTGCCACCACCTGTGTGCAGAGCTT
- Phenotype
-
MIM: 600800
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
NAB1
PubMed Links
Gene Details
- Gene
- NAB1
- Gene Name
- NGFI-A binding protein 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001321312.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
NP_001308241.1 |
NM_001321313.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
NP_001308242.1 |
NM_001321314.1 |
487 |
Intron |
|
|
NP_001308243.1 |
NM_001321315.1 |
487 |
Intron |
|
|
NP_001308244.1 |
NM_005966.3 |
487 |
Intron |
|
|
NP_005957.2 |
XM_005246582.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_005246639.1 |
XM_005246583.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_005246640.1 |
XM_005246586.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_005246643.1 |
XM_005246587.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_005246644.1 |
XM_011511219.2 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_011509521.1 |
XM_017004170.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_016859659.1 |
XM_017004171.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_016859660.1 |
XM_017004172.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_016859661.1 |
XM_017004173.1 |
487 |
Intron |
|
|
XP_016859662.1 |
XM_017004174.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_016859663.1 |
XM_017004175.1 |
487 |
Intron |
|
|
XP_016859664.1 |
XM_017004176.1 |
487 |
Missense Mutation |
CCT,GCT |
P131A |
XP_016859665.1 |
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