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GTTCTCTGCCATGGTAACCTTTGTA[A/G]GCTGGCTGAGTGCCCTCGTGAGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605924 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WDR4 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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WDR4 - WD repeat domain 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001260474.1 | Intron | NP_001247403.1 | ||||
NM_001260475.1 | Intron | NP_001247404.1 | ||||
NM_001260476.1 | Intron | NP_001247405.1 | ||||
NM_001260477.1 | Intron | NP_001247406.1 | ||||
NM_018669.5 | Intron | NP_061139.2 | ||||
NM_033661.4 | Intron | NP_387510.1 | ||||
XM_011529433.1 | Intron | XP_011527735.1 | ||||
XM_017028262.1 | Intron | XP_016883751.1 | ||||
XM_017028263.1 | Intron | XP_016883752.1 | ||||
XM_017028264.1 | Intron | XP_016883753.1 |