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GCGCTTTTGGGAGAGCTACATCTAC[A/G]ATGGCAAAGGAGGTGAGTGAGGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616759 MIM: 616633 MIM: 604429 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NOSIP 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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NOSIP - nitric oxide synthase interacting protein | ||||||
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There are no transcripts associated with this gene. |
PRR12 - proline rich 12 | ||||||
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There are no transcripts associated with this gene. |
PRRG2 - proline rich and Gla domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000951.2 | 621 | Missense Mutation | AAT,GAT | N,D 97 | NP_000942.1 | |
NM_001316335.1 | 621 | Missense Mutation | AAT,GAT | N,D 74 | NP_001303264.1 | |
XM_006723286.2 | 621 | Missense Mutation | AAT,GAT | N,D 97 | XP_006723349.1 | |
XM_011527124.1 | 621 | Missense Mutation | AAT,GAT | N,D 74 | XP_011525426.1 |