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TTCAAACTCAGCTGACTGTTGGTCA[A/G]AGGTAAGTCTTGGTCCAGTAAGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611314 MIM: 602095 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HMGN2P46 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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HMGN2P46 - high mobility group nucleosomal binding domain 2 pseudogene 46 | ||||||
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There are no transcripts associated with this gene. |
SLC30A4 - solute carrier family 30 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321036.1 | 365 | Silent Mutation | CTG,TTG | L,L 83 | NP_001307965.1 | |
NM_013309.5 | 365 | Silent Mutation | CTG,TTG | L,L 83 | NP_037441.2 | |
XM_011521997.2 | 365 | Silent Mutation | CTG,TTG | L,L 83 | XP_011520299.1 | |
XM_017022560.1 | 365 | Silent Mutation | CTG,TTG | L,L 83 | XP_016878049.1 | |
XM_017022561.1 | 365 | Silent Mutation | CTG,TTG | L,L 83 | XP_016878050.1 | |
XM_017022562.1 | 365 | Silent Mutation | CTG,TTG | L,L 83 | XP_016878051.1 |