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GTAAGCATTCGGATCTTCCTGAGAC[C/T]GAGTCACCACCTTGAACTGGCGCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131340 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC727993 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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LOC727993 - uncharacterized LOC727993 | ||||||
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There are no transcripts associated with this gene. |
PDYN - prodynorphin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001190892.1 | 991 | Missense Mutation | NP_001177821.1 | |||
NM_001190898.2 | 991 | Missense Mutation | NP_001177827.1 | |||
NM_001190899.2 | 991 | Missense Mutation | NP_001177828.1 | |||
NM_001190900.1 | 991 | Missense Mutation | NP_001177829.1 | |||
NM_024411.4 | 991 | Missense Mutation | NP_077722.1 | |||
XM_011529244.1 | 991 | Missense Mutation | XP_011527546.1 | |||
XM_011529245.1 | 991 | Missense Mutation | XP_011527547.1 | |||
XM_011529246.2 | 991 | Missense Mutation | XP_011527548.1 | |||
XM_011529247.1 | 991 | Missense Mutation | XP_011527549.1 | |||
XM_011529248.1 | 991 | Missense Mutation | XP_011527550.1 | |||
XM_011529249.2 | 991 | Missense Mutation | XP_011527551.1 | |||
XM_011529250.2 | 991 | Missense Mutation | XP_011527552.1 | |||
XM_017027878.1 | 991 | Missense Mutation | XP_016883367.1 |