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TTCTAACCAATAAGAGATGGCTTTA[C/T]GTCTAGCTAATATCATGGCGACAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603575 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NME5 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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NME5 - NME/NM23 family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003551.2 | 265 | Missense Mutation | CAT,CGT | H,R 87 | NP_003542.1 | |
XM_005272099.1 | 265 | Missense Mutation | CAT,CGT | H,R 87 | XP_005272156.1 | |
XM_006714716.3 | 265 | Missense Mutation | CAT,CGT | H,R 87 | XP_006714779.1 | |
XM_017009945.1 | 265 | Missense Mutation | CAT,CGT | H,R 87 | XP_016865434.1 |