List of variants in gene SEPSECS reported as uncertain significance by Natera, Inc.

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_016955.4(SEPSECS):c.919A>G (p.Ser307Gly)	rs150309842	0.00099
NM_016955.4(SEPSECS):c.548-1G>A	rs200041461	0.00014
NM_016955.4(SEPSECS):c.1027-7G>A	rs374407543	0.00011
NM_016955.4(SEPSECS):c.388+10G>A	rs376797370	0.00011
NM_016955.4(SEPSECS):c.1291T>G (p.Cys431Gly)	rs572892329	0.00009
NM_016955.4(SEPSECS):c.584G>A (p.Gly195Asp)	rs139718374	0.00009
NM_016955.4(SEPSECS):c.960A>G (p.Leu320=)	rs141199115	0.00009
NM_016955.4(SEPSECS):c.1027-9T>C	rs368335778	0.00008
NM_016955.4(SEPSECS):c.1212-10C>G	rs375688949	0.00008
NM_016955.4(SEPSECS):c.*6G>A	rs753956739	0.00007
NM_016955.4(SEPSECS):c.1320C>T (p.Ile440=)	rs375534729	0.00007
NM_016955.4(SEPSECS):c.1351A>G (p.Ile451Val)	rs764436131	0.00004
NM_016955.4(SEPSECS):c.1250A>G (p.Tyr417Cys)	rs762180254	0.00003
NM_016955.4(SEPSECS):c.1390G>T (p.Glu464Ter)	rs747732980	0.00002
NM_016955.4(SEPSECS):c.264T>A (p.His88Gln)	rs756402081	0.00001
NM_016955.4(SEPSECS):c.389G>A (p.Gly130Asp)	rs1004182733	0.00001
NM_016955.4(SEPSECS):c.1022G>A (p.Arg341Lys)	rs1064796736
NM_016955.4(SEPSECS):c.1120G>A (p.Ala374Thr)	rs1261267969
NM_016955.4(SEPSECS):c.1222C>T (p.Leu408Phe)	rs752082832
NM_016955.4(SEPSECS):c.1453G>A (p.Ala485Thr)	rs1233729947
NM_016955.4(SEPSECS):c.1461A>C (p.Lys487Asn)	rs1728243877
NM_016955.4(SEPSECS):c.491A>G (p.Tyr164Cys)	rs768840152
NM_016955.4(SEPSECS):c.499T>C (p.Trp167Arg)	rs1194507895
NM_016955.4(SEPSECS):c.804+4A>T	rs1479554001

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