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TCAGGATGGATCGGTCTCTTGCTGC[A/G]CCTCTGGGCCATCGTTCCCAGCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604153 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NMUR1 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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NMUR1 - neuromedin U receptor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006056.4 | 1354 | Missense Mutation | GCG,GTG | A,V 419 | NP_006047.3 | |
XM_006712195.3 | 1354 | Intron | XP_006712258.1 | |||
XM_006712196.3 | 1354 | Intron | XP_006712259.1 | |||
XM_011510487.2 | 1354 | Missense Mutation | GCG,GTG | A,V 396 | XP_011508789.1 | |
XM_011510488.2 | 1354 | Intron | XP_011508790.1 | |||
XM_011510489.2 | 1354 | Intron | XP_011508791.1 |