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CTGCGGGAGAGCCGGGTACCGGCCG[T/G]GGAAGCGGCCACCGACTACTGTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616213 | ||||||||||||||||||||
Literature Links: |
ZNF292 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
ZNF292 - zinc finger protein 292 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015021.1 | 159 | Missense Mutation | GGG,GTG | G,V 44 | NP_055836.1 | |
XM_005248697.4 | 159 | Intron | XP_005248754.1 | |||
XM_011535625.2 | 159 | UTR 5 | XP_011533927.1 | |||
XM_017010575.1 | 159 | Intron | XP_016866064.1 | |||
XM_017010576.1 | 159 | Intron | XP_016866065.1 | |||
XM_017010577.1 | 159 | Intron | XP_016866066.1 | |||
XM_017010578.1 | 159 | Intron | XP_016866067.1 | |||
XM_017010579.1 | 159 | Intron | XP_016866068.1 | |||
XM_017010580.1 | 159 | Intron | XP_016866069.1 | |||
XM_017010581.1 | 159 | UTR 5 | XP_016866070.1 | |||
XM_017010582.1 | 159 | Intron | XP_016866071.1 | |||
XM_017010583.1 | 159 | Intron | XP_016866072.1 | |||
XM_017010584.1 | 159 | Intron | XP_016866073.1 |