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CCACGCTGTTGTGTCTGCCCCATTA[C/T]TGGTGTCATTTCTGCAGTATTTGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 162340 MIM: 616144 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NMB 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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NMB - neuromedin B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021077.3 | 791 | UTR 3 | NP_066563.2 | |||
NM_205858.1 | 791 | Missense Mutation | ATA,GTA | I,V 123 | NP_995580.1 | |
XM_017022239.1 | 791 | Intron | XP_016877728.1 |
WDR73 - WD repeat domain 73 | ||||||
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There are no transcripts associated with this gene. |