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CATTTACTTCCCCATGAGTAGGATT[G/T]CAGTTTCCCAAACCTGAGATGATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF394 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 |
ZNF394 - zinc finger protein 394 | ||||||
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There are no transcripts associated with this gene. |
ZNF789 - zinc finger protein 789 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001013258.1 | 531 | Intron | NP_001013276.1 | |||
NM_213603.2 | 531 | Missense Mutation | TTG,TTT | L,F 52 | NP_998768.2 | |
XM_011516067.2 | 531 | Missense Mutation | TTG,TTT | L,F 45 | XP_011514369.1 | |
XM_011516070.2 | 531 | Missense Mutation | TTG,TTT | L,F 35 | XP_011514372.1 | |
XM_011516073.2 | 531 | Intron | XP_011514375.1 | |||
XM_017012018.1 | 531 | Missense Mutation | TTG,TTT | L,F 52 | XP_016867507.1 | |
XM_017012019.1 | 531 | Missense Mutation | TTG,TTT | L,F 35 | XP_016867508.1 | |
XM_017012020.1 | 531 | Missense Mutation | TTG,TTT | L,F 35 | XP_016867509.1 | |
XM_017012021.1 | 531 | Missense Mutation | TTG,TTT | L,F 35 | XP_016867510.1 | |
XM_017012022.1 | 531 | Missense Mutation | TTG,TTT | L,F 35 | XP_016867511.1 | |
XM_017012023.1 | 531 | Intron | XP_016867512.1 | |||
XM_017012024.1 | 531 | UTR 5 | XP_016867513.1 | |||
XM_017012025.1 | 531 | UTR 5 | XP_016867514.1 | |||
XM_017012026.1 | 531 | UTR 5 | XP_016867515.1 | |||
XM_017012027.1 | 531 | UTR 5 | XP_016867516.1 |