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TCTAGGTGCATATAATAGGGAGGTT[A/C]TACCTGACAAGGCTTTGGGAAAGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602952 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
WHSC1 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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
WHSC1 - Wolf-Hirschhorn syndrome candidate 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042424.2 | Intron | NP_001035889.1 | ||||
NM_007331.1 | Intron | NP_015627.1 | ||||
NM_133330.2 | Intron | NP_579877.1 | ||||
NM_133331.2 | Intron | NP_579878.1 | ||||
NM_133334.2 | Intron | NP_579889.1 | ||||
NM_133335.3 | Intron | NP_579890.1 | ||||
XM_005248001.3 | Intron | XP_005248058.1 | ||||
XM_005248002.2 | Intron | XP_005248059.1 | ||||
XM_005248005.2 | Intron | XP_005248062.1 | ||||
XM_006713914.3 | Intron | XP_006713977.1 | ||||
XM_011513557.2 | Intron | XP_011511859.1 | ||||
XM_011513560.2 | Intron | XP_011511862.1 | ||||
XM_017008587.1 | Intron | XP_016864076.1 | ||||
XM_017008588.1 | Intron | XP_016864077.1 |