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CTACGTTCCTGTTTGCGAGGAGGCC[A/G]CTGATGTTTAATGATGTCTGAGGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605422 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF350 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ZNF350 - zinc finger protein 350 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021632.3 | 1815 | Silent Mutation | AGC,AGT | S,S 476 | NP_067645.3 | |
XM_011527196.1 | 1815 | Silent Mutation | AGC,AGT | S,S 440 | XP_011525498.1 | |
XM_017027094.1 | 1815 | Silent Mutation | AGC,AGT | S,S 518 | XP_016882583.1 | |
XM_017027095.1 | 1815 | Silent Mutation | AGC,AGT | S,S 518 | XP_016882584.1 | |
XM_017027096.1 | 1815 | Silent Mutation | AGC,AGT | S,S 518 | XP_016882585.1 | |
XM_017027097.1 | 1815 | Silent Mutation | AGC,AGT | S,S 482 | XP_016882586.1 | |
XM_017027098.1 | 1815 | Silent Mutation | AGC,AGT | S,S 476 | XP_016882587.1 | |
XM_017027099.1 | 1815 | Silent Mutation | AGC,AGT | S,S 476 | XP_016882588.1 | |
XM_017027100.1 | 1815 | Silent Mutation | AGC,AGT | S,S 476 | XP_016882589.1 | |
XM_017027101.1 | 1815 | Silent Mutation | AGC,AGT | S,S 250 | XP_016882590.1 | |
XM_017027102.1 | 1815 | Silent Mutation | AGC,AGT | S,S 250 | XP_016882591.1 | |
XM_017027103.1 | 1815 | Silent Mutation | AGC,AGT | S,S 250 | XP_016882592.1 | |
XM_017027104.1 | 1815 | Silent Mutation | AGC,AGT | S,S 250 | XP_016882593.1 |
ZNF350-AS1 - ZNF350 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |