Variant #0001076066 (NC_000021.8:g.45941909C>T, NM_144991.2:c.1423G>A (TSPEAR))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45941909C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSPEAR_000073
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs782056388
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-05-06 10:07:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSPEAR NM_144991.2 +?/. - c.1423G>A r.(?) p.(Gly475Ser)


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