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AAAAGTGGAGGTAACTGATTCTTGG[G/C]GAGCGGAGTTCACTGCTGCCCAGTG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 656 | Silent Mutation | TCC,TCG | S,S 93 | NP_001135946.1 | |
NM_001142475.1 | 656 | Silent Mutation | TCC,TCG | S,S 103 | NP_001135947.1 | |
NM_001142476.1 | 656 | Silent Mutation | TCC,TCG | S,S 59 | NP_001135948.1 | |
NM_001142477.1 | 656 | Intron | NP_001135949.1 | |||
NM_001142478.1 | 656 | Intron | NP_001135950.1 | |||
NM_001142479.1 | 656 | Intron | NP_001135951.1 | |||
NM_001142480.1 | 656 | Intron | NP_001135952.1 | |||
NM_001142481.1 | 656 | Intron | NP_001135953.1 | |||
NM_001142482.1 | 656 | Intron | NP_001135954.1 | |||
NM_001142483.1 | 656 | Silent Mutation | TCC,TCG | S,S 59 | NP_001135955.1 | |
NM_004772.2 | 656 | Intron | NP_004763.1 | |||
XM_006714732.1 | 656 | Intron | XP_006714795.1 | |||
XM_006714733.2 | 656 | Silent Mutation | TCC,TCG | S,S 78 | XP_006714796.1 |
STARD4-AS1 - STARD4 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |