List of variants in gene combination FBXO11, MSH6 reported by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.2392AAC[1] (p.Asn799del)	rs2104626104
NM_001190274.2(FBXO11):c.2520_2521del (p.Ser841fs)	rs2104621655
NM_001190274.2(FBXO11):c.2568_2572del (p.Asn857fs)	rs2104613365
NM_001190274.2(FBXO11):c.2570_2572del (p.Asn857del)	rs2104613345
NM_001190274.2(FBXO11):c.2592_2593del (p.Ile864fs)	rs2104613193
NM_001190274.2(FBXO11):c.2685_2686del (p.Leu895_Ser896insTer)	rs1572753822
NM_001190274.2(FBXO11):c.2688_2699del (p.Asn897_Thr900del)	rs2104611165
NM_001190274.2(FBXO11):c.2729A>T (p.Asp910Val)	rs1670355281
NM_001190274.2(FBXO11):c.2738_2739del (p.Leu912_Tyr913insTer)	rs1553334863
NM_001190274.2(FBXO11):c.2748_2749del (p.Pro917fs)	rs2104610531

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