Variant (rsID / SNP)

rs142638391

rs142638391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ESPN. Location: chromosome 1, position 6,504,654. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ESPNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:6504654
Cytoband: 1p36.31
HGVS: NM_031475.3(ESPN):c.1104T>G (p.Phe368Leu)
Allele change: Missense_F368L

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.