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TTGAGCCTGTTGAATCCAGAAGGAC[A/G]GAAGTCTTGGTAACGGTGTCAGGCT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613663 | |||||||||||||||||||||||
Literature Links: |
SHQ1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
SHQ1 - SHQ1, H/ACA ribonucleoprotein assembly factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018130.2 | Intron | NP_060600.2 | ||||
XM_011533895.2 | Intron | XP_011532197.1 | ||||
XM_011533896.2 | Intron | XP_011532198.1 | ||||
XM_011533897.2 | Intron | XP_011532199.1 | ||||
XM_011533898.2 | Intron | XP_011532200.1 | ||||
XM_011533899.1 | Intron | XP_011532201.1 | ||||
XM_017006724.1 | Intron | XP_016862213.1 |