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GACCTCCCGGGCTCAAGCAGTCCTC[C/T]GTCCCACCTCAGCCTTCTGAGGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
N4BP3 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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N4BP3 - NEDD4 binding protein 3 | ||||||
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There are no transcripts associated with this gene. |
RMND5B - required for meiotic nuclear division 5 homolog B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288794.1 | 318 | UTR 5 | NP_001275723.1 | |||
NM_001288795.1 | 318 | Missense Mutation | CCG,CTG | P,L 15 | NP_001275724.1 | |
NM_022762.4 | 318 | Intron | NP_073599.2 | |||
XM_005265969.3 | 318 | Intron | XP_005266026.1 | |||
XM_005265971.4 | 318 | Intron | XP_005266028.1 | |||
XM_005265972.3 | 318 | Intron | XP_005266029.1 | |||
XM_017009727.1 | 318 | Intron | XP_016865216.1 | |||
XM_017009728.1 | 318 | Intron | XP_016865217.1 |