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CTGACCCCTCCACGTCATGAACACT[A/G]AGTAGCTCCTGACACTGCTTATGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610697 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PDZD2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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PDZD2 - PDZ domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178140.3 | Intron | NP_835260.2 | ||||
XM_005248269.4 | Intron | XP_005248326.1 | ||||
XM_005248271.1 | Intron | XP_005248328.1 | ||||
XM_005248272.3 | Intron | XP_005248329.1 | ||||
XM_006714460.2 | Intron | XP_006714523.1 | ||||
XM_011513992.2 | Intron | XP_011512294.1 | ||||
XM_011513993.2 | Intron | XP_011512295.1 | ||||
XM_011513994.2 | Intron | XP_011512296.1 | ||||
XM_011513995.2 | Intron | XP_011512297.1 | ||||
XM_011513996.2 | Intron | XP_011512298.1 | ||||
XM_017009245.1 | Intron | XP_016864734.1 | ||||
XM_017009246.1 | Intron | XP_016864735.1 |
Set Membership: |
HapMap |