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CCTCCCTCACTCAGTCATTGTCTGG[A/G]AACAGCCCATGAGAAAGCACAGCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608151 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WDR19 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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WDR19 - WD repeat domain 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317924.1 | Intron | NP_001304853.1 | ||||
NM_025132.3 | Intron | NP_079408.3 | ||||
XM_011513724.1 | Intron | XP_011512026.1 | ||||
XM_011513725.2 | Intron | XP_011512027.1 | ||||
XM_011513726.2 | Intron | XP_011512028.1 | ||||
XM_011513727.1 | Intron | XP_011512029.1 | ||||
XM_017008501.1 | Intron | XP_016863990.1 |