Variant (rsID / SNP)

rs10028124

rs10028124 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCLT1. Location: chromosome 4, position 129,867,280. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SCLT1Not classified

Variant type: missense_variant
Chromosome / position: 4:129867280
HGVS: NM_144643.4,c.1321A>T,p.Ser441Cys
Allele change: Missense_S441C

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.