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GAAAGGCGAGGAGCCATGGATATTA[C/G]AGGAAAAATTTCCAAGCCAGAGTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616085 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF37A 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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ZNF37A - zinc finger protein 37A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007094.2 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001007095.1 | |
NM_001178101.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001171572.1 | |
NM_001324245.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311174.1 | |
NM_001324246.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311175.1 | |
NM_001324247.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311176.1 | |
NM_001324248.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311177.1 | |
NM_001324249.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311178.1 | |
NM_001324250.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311179.1 | |
NM_001324251.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311180.1 | |
NM_001324252.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311181.1 | |
NM_001324253.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311182.1 | |
NM_001324254.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311183.1 | |
NM_001324256.1 | 768 | Intron | NP_001311185.1 | |||
NM_001324257.1 | 768 | Intron | NP_001311186.1 | |||
NM_001324258.1 | 768 | Intron | NP_001311187.1 | |||
NM_001324259.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311188.1 | |
NM_001324260.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311189.1 | |
NM_001324261.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311190.1 | |
NM_001324262.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | NP_001311191.1 | |
NM_003421.2 | 768 | Intron | NP_003412.1 | |||
XM_005252586.3 | 768 | Intron | XP_005252643.1 | |||
XM_011519656.2 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | XP_011517958.1 | |
XM_011519657.2 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | XP_011517959.1 | |
XM_011519658.2 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | XP_011517960.1 | |
XM_017016618.1 | 768 | UTR 5 | XP_016872107.1 | |||
XM_017016619.1 | 768 | UTR 5 | XP_016872108.1 | |||
XM_017016620.1 | 768 | UTR 5 | XP_016872109.1 | |||
XM_017016621.1 | 768 | Intron | XP_016872110.1 | |||
XM_017016622.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | XP_016872111.1 | |
XM_017016623.1 | 768 | Intron | XP_016872112.1 | |||
XM_017016624.1 | 768 | Missense Mutation | CAG,GAG | Q,E 70 | XP_016872113.1 |