List of variants in gene combination TP53, WRAP53 studied for not specified

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001143992.2(WRAP53):c.202C>G (p.Arg68Gly)	rs2287499	0.32078
NM_001143992.2(WRAP53):c.450C>T (p.Phe150=)	rs2287498	0.13667
NM_001143992.2(WRAP53):c.31C>T (p.Pro11Ser)	rs17880282	0.02475
NM_001143992.2(WRAP53):c.407C>G (p.Pro136Arg)	rs34067256	0.00138
NM_001143992.2(WRAP53):c.187G>A (p.Val63Met)	rs145760222	0.00021
NM_001143992.2(WRAP53):c.1A>G (p.Met1Val)	rs867179605	0.00017
NM_001143992.2(WRAP53):c.560A>C (p.Asn187Thr)	rs35762939	0.00003
NM_001143992.2(WRAP53):c.350A>C (p.Glu117Ala)	rs148728256	0.00001
NM_001143992.2(WRAP53):c.621G>A (p.Glu207=)	rs200805760	0.00001
NM_001143992.2(WRAP53):c.335G>A (p.Ser112Asn)	rs766695794
NM_001143992.2(WRAP53):c.431C>G (p.Thr144Ser)	rs1156897458

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