Variant #0001067277 (NC_000019.9:g.56001026G>A, NM_001144950.1:c.358G>A (SSC5D))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56001026G>A
DNA change (hg38) -
Published as SSC5D(NM_001144950.2):c.358G>A (p.(Ala120Thr))
ISCN -
DB-ID NAT14_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00079 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SSC5D NM_001144950.1 ?/. - c.358G>A r.(?) p.(Ala120Thr)
NAT14 NM_020378.3 ?/. - c.*2703G>A r.(=) p.(=)


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