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TCCTCTATTATGTAGCACATTTAAT[A/G]TTTTGAATTCTAATGGCATTCTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602547 | ||||||||||||||||||||
Literature Links: |
MIR548P PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MIR548P - microRNA 548p | ||||||
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There are no transcripts associated with this gene. |
ST8SIA4 - ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005668.5 | 1346 | Missense Mutation | ACA,ATA | T,I 339 | NP_005659.1 | |
NM_175052.2 | 1346 | Intron | NP_778222.1 | |||
XM_005272078.2 | 1346 | Intron | XP_005272135.1 | |||
XM_011543630.1 | 1346 | Missense Mutation | ACA,ATA | T,I 241 | XP_011541932.1 |