Variant ID | 25631 |
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Entrez Gene ID | 101927186 |
Gene | ADGRL3-AS1 (GeneCards) |
Location | hg19 4:63987059-63987059
hg38 4:63121341-63121341 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000004.11:g.63987059 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 | 191154276 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.8501 |
CADD Raw score (version 1.3) | -0.926287 (Deleterious) |
FATHMM raw prediction score | 0.02823 (Tolerated) |
Deleterious probability by DeFine | 0.1389 (Neutral) |
Entrez Gene ID | 101927186 (NCBI Gene) |
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Official Gene Symbol | ADGRL3-AS1 (GeneCards) |
Number of variants in ADGRL3-AS1 in this database | 34 (view all the variants) |
Full name | adhesion G protein-coupled receptor L3 antisense RNA 1 |
Band | 4q13.1 |
Other IDs | HGNC: HGNC:50604 |
Other names | LPHN3-AS1 |
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 |