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GCGAGGAGGCCGCTGATGTTTAATG[A/G]TGTCTGAGGGGCCACAGAAGGCACT
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 | ||||||
---|---|---|---|---|---|---|---|---|
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) - Not Available | ||||||
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 | 1801 | Missense Mutation | CCA,TCA | P,S 472 | NP_067645.3 | |
XM_011527196.1 | 1801 | Missense Mutation | CCA,TCA | P,S 436 | XP_011525498.1 | |
XM_017027094.1 | 1801 | Missense Mutation | CCA,TCA | P,S 514 | XP_016882583.1 | |
XM_017027095.1 | 1801 | Missense Mutation | CCA,TCA | P,S 514 | XP_016882584.1 | |
XM_017027096.1 | 1801 | Missense Mutation | CCA,TCA | P,S 514 | XP_016882585.1 | |
XM_017027097.1 | 1801 | Missense Mutation | CCA,TCA | P,S 478 | XP_016882586.1 | |
XM_017027098.1 | 1801 | Missense Mutation | CCA,TCA | P,S 472 | XP_016882587.1 | |
XM_017027099.1 | 1801 | Missense Mutation | CCA,TCA | P,S 472 | XP_016882588.1 | |
XM_017027100.1 | 1801 | Missense Mutation | CCA,TCA | P,S 472 | XP_016882589.1 | |
XM_017027101.1 | 1801 | Missense Mutation | CCA,TCA | P,S 246 | XP_016882590.1 | |
XM_017027102.1 | 1801 | Missense Mutation | CCA,TCA | P,S 246 | XP_016882591.1 | |
XM_017027103.1 | 1801 | Missense Mutation | CCA,TCA | P,S 246 | XP_016882592.1 | |
XM_017027104.1 | 1801 | Missense Mutation | CCA,TCA | P,S 246 | XP_016882593.1 |
ZNF350-AS1 - ZNF350 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |