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TTTTGCTACGGGCCCTAGACAATAC[A/G]ATGGAACGTTCTATGAATTTCGTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608871 MIM: 608872 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NIPSNAP3A 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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NIPSNAP3A - nipsnap homolog 3A | ||||||
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There are no transcripts associated with this gene. |
NIPSNAP3B - nipsnap homolog 3B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018376.3 | 597 | Missense Mutation | AAT,GAT | N,D 33 | NP_060846.2 | |
XM_011518839.1 | 597 | Missense Mutation | AAT,GAT | N,D 33 | XP_011517141.1 | |
XM_017014889.1 | 597 | Missense Mutation | AAT,GAT | N,D 33 | XP_016870378.1 |