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GCAGAGGAAGAGCGTGTCCACACAC[A/G]TGCCGAAAACGCTGAAGAAGCCGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608272 MIM: 606107 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NEU1 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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NEU1 - neuraminidase 1 (lysosomal sialidase) | ||||||
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There are no transcripts associated with this gene. |
SLC44A4 - solute carrier family 44 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001178044.1 | 2051 | Missense Mutation | ACG,ATG | T,M 619 | NP_001171515.1 | |
NM_001178045.1 | 2051 | Missense Mutation | ACG,ATG | T,M 585 | NP_001171516.1 | |
NM_025257.2 | 2051 | Missense Mutation | ACG,ATG | T,M 661 | NP_079533.2 |