GENETIC ENCYCLOPEDIA
ABOUT US    

   

NM_015046.7(SETX):c.4156A>G (p.Ile1386Val) AND not specified

Significance: Benign
ClinVar: RCV000081696

Variant: NM_015046.7(SETX):c.4156A>G (p.Ile1386Val)

Type: Variant
Allele: NM_015046.7(SETX):c.4156A>G (p.Ile1386Val) 101560
Gene:
Type: single nucleotide variant
Location: Chr9: 132327442 - assembly GRCh38
Chr9: 135202829 - assembly GRCh37
References: dbSNP: 543573
UniProtKB: Q7Z333#VAR_018787
Illumina Clinical Services Laboratory,Illumina: 46680

Condition

Disease: not specified