List of variants in gene SLC35A2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_005660.3(SLC35A2):c.1078G>A (p.Val360Ile)	rs138190020	0.00045
NM_005660.3(SLC35A2):c.30C>G (p.Thr10=)	rs373480204	0.00041
NM_005660.3(SLC35A2):c.12T>G (p.Val4=)	rs782793880	0.00023
NM_005660.3(SLC35A2):c.447C>A (p.Ile149=)	rs782379632	0.00011
NM_005660.3(SLC35A2):c.1039G>A (p.Ala347Thr)	rs781948153	0.00006
NM_005660.3(SLC35A2):c.615C>T (p.Ala205=)	rs781922248	0.00006
NM_005660.3(SLC35A2):c.1062C>T (p.Ser354=)	rs142781476	0.00004
NM_005660.3(SLC35A2):c.818G>C (p.Gly273Ala)	rs1557042798	0.00001
NM_005660.3(SLC35A2):c.*32G>A
NM_005660.3(SLC35A2):c.1042A>G (p.Ile348Val)
NM_005660.3(SLC35A2):c.1163+105G>A
NM_005660.3(SLC35A2):c.177G>C (p.Thr59=)	rs782621918
NM_005660.3(SLC35A2):c.288C>T (p.His96=)
NM_005660.3(SLC35A2):c.439C>T (p.Leu147=)
NM_005660.3(SLC35A2):c.702C>T (p.Arg234=)

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