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TTGGAAATGGTTCTTGACTGACCCA[C/G]ACAAAGAGTTCTGGGTAATAAACCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607332 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NREP 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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NREP - neuronal regeneration related protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142474.1 | 506 | Silent Mutation | GTC,GTG | V,V 43 | NP_001135946.1 | |
NM_001142475.1 | 506 | Silent Mutation | GTC,GTG | V,V 53 | NP_001135947.1 | |
NM_001142476.1 | 506 | Silent Mutation | GTC,GTG | V,V 9 | NP_001135948.1 | |
NM_001142477.1 | 506 | Intron | NP_001135949.1 | |||
NM_001142478.1 | 506 | Intron | NP_001135950.1 | |||
NM_001142479.1 | 506 | Intron | NP_001135951.1 | |||
NM_001142480.1 | 506 | Intron | NP_001135952.1 | |||
NM_001142481.1 | 506 | Intron | NP_001135953.1 | |||
NM_001142482.1 | 506 | Intron | NP_001135954.1 | |||
NM_001142483.1 | 506 | Silent Mutation | GTC,GTG | V,V 9 | NP_001135955.1 | |
NM_004772.2 | 506 | Intron | NP_004763.1 | |||
XM_006714732.1 | 506 | Intron | XP_006714795.1 | |||
XM_006714733.2 | 506 | Silent Mutation | GTC,GTG | V,V 28 | XP_006714796.1 |
STARD4-AS1 - STARD4 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |