Variant ID | 29011 |
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Entrez Gene ID | 389906 |
Gene | LOC389906 (GeneCards) |
Location | hg19 X:4363239-4363239
hg38 X:4445198-4445198 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000023.10:g.4363239 T>C (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 155270560 |
MAF in gnomAD genome (version 2.0.1) | 0.0805 |
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SNP ID (dbSNP ID version 137) | rs34754145 |
CADD Raw score (version 1.3) | -0.081874 (Deleterious) |
FATHMM raw prediction score | 0.0713 (Tolerated) |
Deleterious probability by DeFine | 0.0751 (Neutral) |
Entrez Gene ID | 389906 (NCBI Gene) |
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Official Gene Symbol | LOC389906 (GeneCards) |
Number of variants in LOC389906 in this database | 5 (view all the variants) |
Full name | zinc finger protein 839 pseudogene |
Band | Xp22.33 |
Other IDs | None: |
Other names | None |
Summary | None |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |