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CTATCGCCCATTCGCCCCAGGTGGT[A/G]CAAAGGATCAAGGCTGTGGAGGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607997 MIM: 606553 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NPW PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NPW - neuropeptide W | ||||||
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There are no transcripts associated with this gene. |
SLC9A3R2 - SLC9A3 regulator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130012.2 | 357 | Silent Mutation | GTA,GTG | V,V 73 | NP_001123484.1 | |
NM_001252073.1 | 357 | Intron | NP_001239002.1 | |||
NM_001252075.1 | 357 | Intron | NP_001239004.1 | |||
NM_001252076.1 | 357 | Intron | NP_001239005.1 | |||
NM_004785.5 | 357 | Silent Mutation | GTA,GTG | V,V 73 | NP_004776.3 | |
XM_005255702.4 | 357 | Intron | XP_005255759.1 | |||
XM_006720981.1 | 357 | Intron | XP_006721044.1 | |||
XM_017023894.1 | 357 | Intron | XP_016879383.1 | |||
XM_017023895.1 | 357 | Silent Mutation | GTA,GTG | V,V 17 | XP_016879384.1 |