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TTTTGCTGTGCTTCTGCTTCCTGGT[C/G]TTGTGTAAGTCCCAATTCACTCTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613114 MIM: 608694 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM134B 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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FAM134B - family with sequence similarity 134 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001034850.2 | 1569 | Missense Mutation | CAC,GAC | H,D 475 | NP_001030022.1 | |
NM_019000.4 | 1569 | Missense Mutation | CAC,GAC | H,D 334 | NP_061873.2 | |
XM_011514053.2 | 1569 | Missense Mutation | CAC,GAC | H,D 515 | XP_011512355.1 | |
XM_011514054.2 | 1569 | Missense Mutation | CAC,GAC | H,D 374 | XP_011512356.1 | |
XM_011514055.2 | 1569 | Missense Mutation | CAC,GAC | H,D 342 | XP_011512357.1 |
ZNF622 - zinc finger protein 622 | ||||||
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There are no transcripts associated with this gene. |