chr1-158611131-G-GCACACACACACACACA
Variant summary
Our verdict is Uncertain significance. Variant got 0 ACMG points: 0P and 0B.
The NM_003126.4(SPTA1):c.*117_*132dupTGTGTGTGTGTGTGTG variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.
Frequency
Genomes: 𝑓 0.00041 ( 1 hom., cov: 0)
Exomes 𝑓: 0.00024 ( 1 hom. )
Consequence
SPTA1
NM_003126.4 3_prime_UTR
NM_003126.4 3_prime_UTR
Scores
Not classified
Clinical Significance
Not reported in ClinVar
Conservation
PhyloP100: 0.00
Genes affected
SPTA1 (HGNC:11272): (spectrin alpha, erythrocytic 1) This gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [provided by RefSeq, Aug 2017]
OR10Z1 (HGNC:14996): (olfactory receptor family 10 subfamily Z member 1) Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
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ACMG classification
Classification made for transcript
Verdict is Uncertain_significance. Variant got 0 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
SPTA1 | NM_003126.4 | c.*117_*132dupTGTGTGTGTGTGTGTG | 3_prime_UTR_variant | Exon 52 of 52 | ENST00000643759.2 | NP_003117.2 | ||
OR10Z1 | NM_001004478.2 | c.*3771_*3786dupACACACACACACACAC | 3_prime_UTR_variant | Exon 2 of 2 | ENST00000641002.1 | NP_001004478.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | Exon rank | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
SPTA1 | ENST00000643759 | c.*117_*132dupTGTGTGTGTGTGTGTG | 3_prime_UTR_variant | Exon 52 of 52 | NM_003126.4 | ENSP00000495214.1 | ||||
OR10Z1 | ENST00000641002.1 | c.*3771_*3786dupACACACACACACACAC | 3_prime_UTR_variant | Exon 2 of 2 | NM_001004478.2 | ENSP00000493003.1 | ||||
SPTA1 | ENST00000485680.1 | n.*61_*76dupTGTGTGTGTGTGTGTG | downstream_gene_variant | 3 |
Frequencies
GnomAD3 genomes AF: 0.000410 AC: 59AN: 143812Hom.: 1 Cov.: 0
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GnomAD4 exome AF: 0.000241 AC: 127AN: 527488Hom.: 1 Cov.: 0 AF XY: 0.000239 AC XY: 67AN XY: 279970
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GnomAD4 genome AF: 0.000410 AC: 59AN: 143922Hom.: 1 Cov.: 0 AF XY: 0.000417 AC XY: 29AN XY: 69578
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ClinVar
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Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at