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CTGCCTGCAGCTCGATCTGCAGGAC[A/G]TTCTCCTGGTCTACCTGAACCGGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LOC105371038 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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LOC105371038 - uncharacterized LOC105371038 | ||||||
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There are no transcripts associated with this gene. |
MCRIP2 - MAPK regulated corepressor interacting protein 2 | ||||||
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There are no transcripts associated with this gene. |
WDR90 - WD repeat domain 90 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_145294.4 | 505 | Missense Mutation | ATT,GTT | I,V 151 | NP_660337.3 | |
XM_017023023.1 | 505 | Missense Mutation | ATT,GTT | I,V 151 | XP_016878512.1 | |
XM_017023024.1 | 505 | Intron | XP_016878513.1 |