List of variants in gene LRPPRC reported by CeGaT Center for Human Genetics Tuebingen

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_133259.4(LRPPRC):c.2481A>G (p.Pro827=)	rs115993634	0.00825
NM_133259.4(LRPPRC):c.*399G>A	rs149268737	0.00473
NM_133259.4(LRPPRC):c.149+20C>G	rs540850536	0.00451
NM_133259.4(LRPPRC):c.1529C>G (p.Ala510Gly)	rs115693730	0.00414
NM_133259.4(LRPPRC):c.3034C>T (p.Pro1012Ser)	rs113374262	0.00239
NM_133259.4(LRPPRC):c.1301G>A (p.Gly434Asp)	rs146515622	0.00102
NM_133259.4(LRPPRC):c.1928A>G (p.His643Arg)	rs148575027	0.00074
NM_133259.4(LRPPRC):c.1426A>G (p.Thr476Ala)	rs115507225	0.00066
NM_133259.4(LRPPRC):c.1678A>T (p.Ile560Leu)	rs144826521	0.00058
NM_133259.4(LRPPRC):c.2020G>A (p.Glu674Lys)	rs149243712	0.00039
NM_133259.4(LRPPRC):c.66C>T (p.Leu22=)	rs769158010	0.00026
NM_133259.4(LRPPRC):c.1929C>T (p.His643=)	rs200017171	0.00019
NM_133259.4(LRPPRC):c.802G>C (p.Asp268His)	rs756849117	0.00007
NM_133259.4(LRPPRC):c.2028A>G (p.Gln676=)	rs1309745023	0.00001
NM_133259.4(LRPPRC):c.3648C>T (p.Phe1216=)	rs370683872	0.00001
NC_000002.12:g.43996149G>A
NM_133259.4(LRPPRC):c.1438_1456dup
NM_133259.4(LRPPRC):c.1440_1456dup
NM_133259.4(LRPPRC):c.1456_1457insTTTTTTTTTTTTTTTTTTTTTTTT
NM_133259.4(LRPPRC):c.1936G>T (p.Val646Phe)	rs752968314
NM_133259.4(LRPPRC):c.2280G>A (p.Lys760=)	rs762970067
NM_133259.4(LRPPRC):c.254G>C (p.Trp85Ser)	rs1453934366
NM_133259.4(LRPPRC):c.3279G>A (p.Ala1093=)
NM_133259.4(LRPPRC):c.3323G>T (p.Ser1108Ile)	rs1572900944
NM_133259.4(LRPPRC):c.3342A>G (p.Gln1114=)	rs1572900912
NM_133259.4(LRPPRC):c.3963C>A (p.Tyr1321Ter)	rs863224052
NM_133259.4(LRPPRC):c.7G>A (p.Ala3Thr)	rs200686732

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