List of variants in gene SAMD9L studied for monosomy 7 myelodysplasia and leukemia syndrome 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_152703.5(SAMD9L):c.3102T>C (p.Asp1034=)	rs75823828	0.01398
NM_152703.5(SAMD9L):c.3964T>C (p.Leu1322=)	rs73710962	0.00818
NM_152703.5(SAMD9L):c.1216C>T (p.Arg406Ter)	rs150070697	0.00229
NM_152703.5(SAMD9L):c.2069G>A (p.Gly690Asp)	rs147903234	0.00041
NM_152703.5(SAMD9L):c.4259G>A (p.Ser1420Asn)	rs116662173	0.00024
NM_152703.5(SAMD9L):c.4298T>C (p.Leu1433Pro)	rs146611034	0.00015
NM_152703.5(SAMD9L):c.2114A>G (p.Tyr705Cys)	rs144236612	0.00009
NM_152703.5(SAMD9L):c.1015C>A (p.Leu339Ile)	rs138238924	0.00007
NM_152703.5(SAMD9L):c.4082T>C (p.Val1361Ala)	rs202162088	0.00006
NM_152703.5(SAMD9L):c.2316T>G (p.Thr772=)	rs201861233	0.00005
NM_152703.5(SAMD9L):c.1096T>C (p.Phe366Leu)
NM_152703.5(SAMD9L):c.1364T>C (p.Val455Ala)	rs751090202
NM_152703.5(SAMD9L):c.2052A>C (p.Glu684Asp)	rs1792278396
NM_152703.5(SAMD9L):c.2483G>A (p.Arg828Gln)
NM_152703.5(SAMD9L):c.2640C>A (p.His880Gln)	rs878855336
NM_152703.5(SAMD9L):c.2734C>G (p.Gln912Glu)
NM_152703.5(SAMD9L):c.2956C>T (p.Arg986Cys)	rs1554341158
NM_152703.5(SAMD9L):c.303del (p.Asn103fs)	rs2116506727
NM_152703.5(SAMD9L):c.3842G>A (p.Arg1281Lys)	rs1792140365
NM_152703.5(SAMD9L):c.385A>C (p.Ile129Leu)
NM_152703.5(SAMD9L):c.4535T>C (p.Val1512Ala)	rs1792087738
NM_152703.5(SAMD9L):c.4654T>A (p.Tyr1552Asn)	rs2116467712

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