Variant ID | 26941 |
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Entrez Gene ID | 26953 |
Gene | RANBP6 (GeneCards) |
Location | hg19 9:6074732-6074732
hg38 9:6074732-6074732 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000009.11:g.6074732 G>T (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 | 141213431 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.2662 |
CADD Raw score (version 1.3) | -0.344689 (Deleterious) |
FATHMM raw prediction score | 0.10698 (Tolerated) |
Deleterious probability by DeFine | 0.128 (Neutral) |
Entrez Gene ID | 26953 (NCBI Gene) |
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Official Gene Symbol | RANBP6 (GeneCards) |
Number of variants in RANBP6 in this database | 5 (view all the variants) |
Full name | RAN binding protein 6 |
Band | 9p24.1 |
Other IDs | Vega: OTTHUMG00000019512 HGNC: HGNC:9851 Ensembl: ENSG00000137040 |
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 |