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ATGACAGTCTCATAGATATCCTGCA[A/T]TACATCATTGTAGAGAGTCTTCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 314997 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF75D 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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ZNF75D - zinc finger protein 75D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001185063.2 | 2629 | Intron | NP_001171992.1 | |||
NM_007131.4 | 2629 | Missense Mutation | ATG,TTG | M,L 264 | NP_009062.2 | |
XM_005262469.1 | 2629 | Missense Mutation | ATG,TTG | M,L 264 | XP_005262526.1 | |
XM_005262471.3 | 2629 | Missense Mutation | ATG,TTG | M,L 57 | XP_005262528.1 | |
XM_011531391.1 | 2629 | Missense Mutation | ATG,TTG | M,L 264 | XP_011529693.1 | |
XM_011531395.2 | 2629 | Missense Mutation | ATG,TTG | M,L 114 | XP_011529697.1 | |
XM_011531396.2 | 2629 | Missense Mutation | ATG,TTG | M,L 96 | XP_011529698.1 | |
XM_011531397.2 | 2629 | Missense Mutation | ATG,TTG | M,L 93 | XP_011529699.1 | |
XM_017029818.1 | 2629 | Missense Mutation | ATG,TTG | M,L 118 | XP_016885307.1 | |
XM_017029819.1 | 2629 | Missense Mutation | ATG,TTG | M,L 130 | XP_016885308.1 | |
XM_017029820.1 | 2629 | Missense Mutation | ATG,TTG | M,L 93 | XP_016885309.1 |