NM_003126.4:c.*117_*132dupTGTGTGTGTGTGTGTG

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

Scores

Not classified

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.00
Variant links:
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]

Genome browser will be placed here

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
SPTA1NM_003126.4 linkc.*117_*132dupTGTGTGTGTGTGTGTG 3_prime_UTR_variant Exon 52 of 52 ENST00000643759.2 NP_003117.2 P02549-1
OR10Z1NM_001004478.2 linkc.*3771_*3786dupACACACACACACACAC 3_prime_UTR_variant Exon 2 of 2 ENST00000641002.1 NP_001004478.1 Q8NGY1A0A126GV63

Ensembl

Gene Transcript HGVSc HGVSp Effect Exon rank TSL MANE Protein Appris UniProt
SPTA1ENST00000643759 linkc.*117_*132dupTGTGTGTGTGTGTGTG 3_prime_UTR_variant Exon 52 of 52 NM_003126.4 ENSP00000495214.1 P02549-1
OR10Z1ENST00000641002.1 linkc.*3771_*3786dupACACACACACACACAC 3_prime_UTR_variant Exon 2 of 2 NM_001004478.2 ENSP00000493003.1 Q8NGY1
SPTA1ENST00000485680.1 linkn.*61_*76dupTGTGTGTGTGTGTGTG downstream_gene_variant 3

Frequencies

GnomAD3 genomes
AF:
0.000410
AC:
59
AN:
143812
Hom.:
1
Cov.:
0
show subpopulations
Gnomad AFR
AF:
0.00117
Gnomad AMI
AF:
0.00
Gnomad AMR
AF:
0.00
Gnomad ASJ
AF:
0.00
Gnomad EAS
AF:
0.00144
Gnomad SAS
AF:
0.00
Gnomad FIN
AF:
0.000109
Gnomad MID
AF:
0.00
Gnomad NFE
AF:
0.0000908
Gnomad OTH
AF:
0.00
GnomAD4 exome
AF:
0.000241
AC:
127
AN:
527488
Hom.:
1
Cov.:
0
AF XY:
0.000239
AC XY:
67
AN XY:
279970
show subpopulations
Gnomad4 AFR exome
AF:
0.000533
Gnomad4 AMR exome
AF:
0.000170
Gnomad4 ASJ exome
AF:
0.0000657
Gnomad4 EAS exome
AF:
0.00134
Gnomad4 SAS exome
AF:
0.000471
Gnomad4 FIN exome
AF:
0.0000328
Gnomad4 NFE exome
AF:
0.000116
Gnomad4 OTH exome
AF:
0.000450
GnomAD4 genome
AF:
0.000410
AC:
59
AN:
143922
Hom.:
1
Cov.:
0
AF XY:
0.000417
AC XY:
29
AN XY:
69578
show subpopulations
Gnomad4 AFR
AF:
0.00117
Gnomad4 AMR
AF:
0.00
Gnomad4 ASJ
AF:
0.00
Gnomad4 EAS
AF:
0.00145
Gnomad4 SAS
AF:
0.00
Gnomad4 FIN
AF:
0.000109
Gnomad4 NFE
AF:
0.0000908
Gnomad4 OTH
AF:
0.00

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs55832242; hg19: chr1-158580921; API