LOVD - Variant listings for SCN9A

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Patient data (#0006322)
Patient ID unknown
Disease n/a
Phenotype additional -
Remarks -
Ref_pat-pheno United States:Sacramento
Inherit -
Consang. -
Fam_Pat -
# Reported 1
Geographic origin -
Ethnic origin -
Gender -
Phenotype/Onset -
Histology -
Submitter Christoph Lossin

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
DB-ID SCN9A_00074
DNA change c.554G>A   (View in UCSC Genome Browser, Ensembl)
Location Exon
Protein p.(Arg185His)
Prot/Location D1/S2-S3in
Exon 5
dbSNP -
Reference dbSNP-rs73969684
Genetic origin -
do not use -
Protein original -
Technique SEQ
Codon -

1 entry in SCN9A

Path.
Allele Descending
Ascending
DB-ID Descending
Ascending
DNA change Descending
Ascending
Location Descending
Ascending
Protein Descending
Ascending
Prot/Location Descending
Ascending
Exon Descending
Ascending
dbSNP Descending
Ascending
Reference Descending
Ascending
Genetic origin Descending
Ascending
do not use Descending
Ascending
Protein original Descending
Ascending
Technique Descending
Ascending
Codon Descending
Ascending
?/? Unknown SCN9A_00074 c.554G>A Exon p.(Arg185His) D1/S2-S3in 5 - dbSNP-rs73969684 - - - SEQ -