Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGTGATGACTTGCAAGATTTGA[A/G]CTCTGCCTGAAGACCTTGCCACACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600398 | ||||||||||||||||||||
Literature Links: |
ZNF160 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 |
ZNF160 - zinc finger protein 160 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102603.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001096073.1 | |
NM_001322125.1 | 2815 | Intron | NP_001309054.1 | |||
NM_001322126.1 | 2815 | Intron | NP_001309055.1 | |||
NM_001322128.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309057.1 | |
NM_001322129.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309058.1 | |
NM_001322130.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309059.1 | |
NM_001322131.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309060.1 | |
NM_001322132.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309061.1 | |
NM_001322133.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309062.1 | |
NM_001322134.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309063.1 | |
NM_001322135.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309064.1 | |
NM_001322136.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_001309065.1 | |
NM_001322137.1 | 2815 | Silent Mutation | AGC,AGT | S,S 765 | NP_001309066.1 | |
NM_001322138.1 | 2815 | Silent Mutation | AGC,AGT | S,S 765 | NP_001309067.1 | |
NM_001322139.1 | 2815 | Silent Mutation | AGC,AGT | S,S 765 | NP_001309068.1 | |
NM_033288.3 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_150630.2 | |
NM_198893.2 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | NP_942596.1 | |
XM_017027445.1 | 2815 | Silent Mutation | AGC,AGT | S,S 820 | XP_016882934.1 | |
XM_017027446.1 | 2815 | Silent Mutation | AGC,AGT | S,S 801 | XP_016882935.1 | |
XM_017027447.1 | 2815 | Intron | XP_016882936.1 | |||
XM_017027448.1 | 2815 | Intron | XP_016882937.1 |