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TGACTGTTGGTCAAAGGTAAGTCTT[G/T]GTCCAGTAAGGAATCATCGTCGGCC
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 353 | Missense Mutation | AAA,CAA | K,Q 79 | NP_001307965.1 | |
NM_013309.5 | 353 | Missense Mutation | AAA,CAA | K,Q 79 | NP_037441.2 | |
XM_011521997.2 | 353 | Missense Mutation | AAA,CAA | K,Q 79 | XP_011520299.1 | |
XM_017022560.1 | 353 | Missense Mutation | AAA,CAA | K,Q 79 | XP_016878049.1 | |
XM_017022561.1 | 353 | Missense Mutation | AAA,CAA | K,Q 79 | XP_016878050.1 | |
XM_017022562.1 | 353 | Missense Mutation | AAA,CAA | K,Q 79 | XP_016878051.1 |