ClinVar Miner

List of variants in gene SARS2 studied for abdominal and pelvic region disorder

Included ClinVar conditions (962):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_001145901.2(SARS2):c.1048T>C (p.Phe350Leu) rs1114167285
NM_001145901.2(SARS2):c.30G>A (p.Trp10Ter) rs145754412
NM_001145901.2(SARS2):c.700C>T (p.Arg234Cys) rs201347156
NM_001145901.2(SARS2):c.922+10TG[2] rs60352446
NM_017827.3(SARS2):c.*341G>C rs374281807
NM_017827.4(SARS2):c.*116C>T
NM_017827.4(SARS2):c.*131C>T
NM_017827.4(SARS2):c.*140C>T rs565577459
NM_017827.4(SARS2):c.*224C>T
NM_017827.4(SARS2):c.*22C>A rs199819134
NM_017827.4(SARS2):c.*22C>T rs199819134
NM_017827.4(SARS2):c.*250A>G
NM_017827.4(SARS2):c.*79G>C rs9403
NM_017827.4(SARS2):c.*99T>G
NM_017827.4(SARS2):c.-12T>C rs730078
NM_017827.4(SARS2):c.-19G>T rs781348902
NM_017827.4(SARS2):c.103A>G (p.Thr35Ala) rs34264048
NM_017827.4(SARS2):c.1160+4T>C rs7508411
NM_017827.4(SARS2):c.1169A>G (p.Asp390Gly) rs727502784
NM_017827.4(SARS2):c.11C>T (p.Ser4Phe)
NM_017827.4(SARS2):c.1292G>A (p.Arg431His)
NM_017827.4(SARS2):c.1315A>T (p.Thr439Ser) rs200202461
NM_017827.4(SARS2):c.1317C>T (p.Thr439=) rs556892787
NM_017827.4(SARS2):c.1321G>A (p.Ala441Thr) rs762422369
NM_017827.4(SARS2):c.1347+10G>A rs376335678
NM_017827.4(SARS2):c.138G>T (p.Glu46Asp)
NM_017827.4(SARS2):c.1404C>A (p.Asn468Lys)
NM_017827.4(SARS2):c.1428C>T (p.Leu476=)
NM_017827.4(SARS2):c.1481C>T (p.Thr494Ile)
NM_017827.4(SARS2):c.175G>C (p.Asp59His) rs886054430
NM_017827.4(SARS2):c.230G>T (p.Arg77Leu)
NM_017827.4(SARS2):c.248C>T (p.Ser83Leu) rs34050897
NM_017827.4(SARS2):c.249G>A (p.Ser83=)
NM_017827.4(SARS2):c.310C>T (p.Arg104Trp) rs144760517
NM_017827.4(SARS2):c.315C>G (p.Ser105Arg)
NM_017827.4(SARS2):c.321G>A (p.Glu107=) rs11544093
NM_017827.4(SARS2):c.353G>A (p.Arg118Gln) rs377601567
NM_017827.4(SARS2):c.364-7C>A rs528674259
NM_017827.4(SARS2):c.373G>A (p.Asp125Asn)
NM_017827.4(SARS2):c.390G>A (p.Gln130=) rs61736057
NM_017827.4(SARS2):c.394-5C>G rs886054429
NM_017827.4(SARS2):c.448G>A (p.Val150Ile)
NM_017827.4(SARS2):c.44G>C (p.Arg15Pro) rs773524954
NM_017827.4(SARS2):c.501G>A (p.Ala167=) rs140304897
NM_017827.4(SARS2):c.534+10G>A rs531462148
NM_017827.4(SARS2):c.535-15G>C rs886054428
NM_017827.4(SARS2):c.589+4G>A rs772644235
NM_017827.4(SARS2):c.590-5T>A rs370612303
NM_017827.4(SARS2):c.654-11C>G rs200300920
NM_017827.4(SARS2):c.679C>T (p.Arg227Trp)
NM_017827.4(SARS2):c.758G>A (p.Arg253Gln) rs185053576
NM_017827.4(SARS2):c.759+4T>C
NM_017827.4(SARS2):c.777G>A (p.Thr259=) rs563299553
NM_017827.4(SARS2):c.794G>C (p.Arg265Pro)
NM_017827.4(SARS2):c.84T>C (p.Asp28=)
NM_017827.4(SARS2):c.862C>T (p.Pro288Ser)
NM_017827.4(SARS2):c.877G>A (p.Asp293Asn)
NM_017827.4(SARS2):c.888G>A (p.Leu296=) rs182484523
NM_017827.4(SARS2):c.900G>A (p.Ala300=)
NM_017827.4(SARS2):c.917-4C>T rs542117712
NM_017827.4(SARS2):c.91A>G (p.Arg31Gly) rs138274440
NM_017827.4(SARS2):c.963-10T>C rs749126576
NM_033362.3(MRPS12):c.-176T>A rs554221329

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