List of variants in gene SAMD9 reported by Counsyl

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_017654.4(SAMD9):c.2T>C (p.Met1Thr)	rs201122403	0.00004
NM_017654.4(SAMD9):c.4558G>T (p.Glu1520Ter)	rs200178876	0.00004
NM_017654.4(SAMD9):c.3381C>A (p.Tyr1127Ter)	rs572380130	0.00003
NM_017654.4(SAMD9):c.132del (p.Val45fs)	rs1554337424
NM_017654.4(SAMD9):c.1800_1801del (p.Glu600fs)	rs375515095
NM_017654.4(SAMD9):c.2509dup (p.Arg837fs)	rs1554337029
NM_017654.4(SAMD9):c.3505C>T (p.Gln1169Ter)	rs1554336918
NM_017654.4(SAMD9):c.3651dup (p.Asp1218Ter)	rs199887936
NM_017654.4(SAMD9):c.4331AAC[1] (p.Gln1445del)	rs755666547

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