List of variants studied for autosomal recessive complex spastic paraplegia type 9B by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_002860.4(ALDH18A1):c.1115C>A (p.Ser372Tyr)	rs3765571	0.01418
NM_002860.4(ALDH18A1):c.1329C>T (p.Ile443=)	rs117709404	0.00134
NM_002860.4(ALDH18A1):c.1867G>A (p.Asp623Asn)	rs770815414	0.00006
NM_002860.4(ALDH18A1):c.1551C>A (p.His517Gln)	rs185313265
NM_002860.4(ALDH18A1):c.1740C>G (p.Ser580Arg)	rs139035272
NM_002860.4(ALDH18A1):c.1780G>A (p.Val594Ile)
NM_002860.4(ALDH18A1):c.1784A>G (p.Asp595Gly)
NM_002860.4(ALDH18A1):c.34C>G (p.Pro12Ala)
NM_002860.4(ALDH18A1):c.86C>T (p.Ser29Phe)

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