Variant ID | 28189 |
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Entrez Gene ID | 51061 |
Gene | TXNDC11 (GeneCards) |
Location | hg19 16:11811725-11811725
hg38 16:11717869-11717869 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000016.9:g.11811725 A>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 | 90354753 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.2105 |
CADD Raw score (version 1.3) | 0.260345 (Deleterious) |
FATHMM raw prediction score | 0.29089 (Tolerated) |
Deleterious probability by DeFine | 0.5515 (Deleterious) |
Entrez Gene ID | 51061 (NCBI Gene) |
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Official Gene Symbol | TXNDC11 (GeneCards) |
Number of variants in TXNDC11 in this database | 3 (view all the variants) |
Full name | thioredoxin domain containing 11 |
Band | 16p13.13 |
Other IDs | Vega: OTTHUMG00000177467 OMIM: 617792 HGNC: HGNC:28030 Ensembl: ENSG00000153066 |
Other names | EFP1 |
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 |