ClinVar Miner

List of variants in gene TNFRSF1A reported as benign for connective tissue disorder

Included ClinVar conditions (343):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001065.4(TNFRSF1A):c.473-33T>C rs1800692 0.70815
NM_001065.4(TNFRSF1A):c.36A>G (p.Pro12=) rs767455 0.39963
NM_001065.4(TNFRSF1A):c.625+10A>G rs1800693 0.38055
NM_001065.4(TNFRSF1A):c.*333G>A rs4149646 0.04651
NM_001065.4(TNFRSF1A):c.362G>A (p.Arg121Gln) rs4149584 0.01206
NM_001065.4(TNFRSF1A):c.224C>T (p.Pro75Leu) rs4149637 0.00574
NM_001065.4(TNFRSF1A):c.1110C>T (p.Arg370=) rs201683984 0.00236
NM_001065.4(TNFRSF1A):c.935G>A (p.Arg312Lys) rs200900510 0.00113
NM_001065.4(TNFRSF1A):c.789T>C (p.Thr263=) rs201290189 0.00069
NM_001065.4(TNFRSF1A):c.1075C>T (p.Leu359=) rs151344628 0.00050
NM_001065.4(TNFRSF1A):c.987C>T (p.Leu329=) rs138261783 0.00047
NM_001065.4(TNFRSF1A):c.645C>T (p.Pro215=) rs147075345 0.00020
NM_001065.4(TNFRSF1A):c.15C>T (p.Thr5=) rs200386529 0.00008
NM_001065.4(TNFRSF1A):c.193+19G>A rs17847989 0.00003
NM_001065.4(TNFRSF1A):c.816C>T (p.Ser272=) rs45562531 0.00002
NM_001065.4(TNFRSF1A):c.1058-16G>A rs765248274 0.00001
NM_001065.4(TNFRSF1A):c.194-18_194-17del rs104895267
NM_001065.4(TNFRSF1A):c.626-32G>T rs200415260
NM_001065.4(TNFRSF1A):c.714G>A (p.Arg238=) rs200376188

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