List of variants in gene MAP2K2 reported as benign for not provided

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 31

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HGVS	dbSNP
NM_030662.3(MAP2K2):c.-206G>T
NM_030662.3(MAP2K2):c.-269G>A
NM_030662.3(MAP2K2):c.-285G>T
NM_030662.3(MAP2K2):c.-366G>A
NM_030662.3(MAP2K2):c.1047-140_1047-139insG
NM_030662.3(MAP2K2):c.1047-279C>T
NM_030662.3(MAP2K2):c.1065G>A (p.Ala355=)	rs374807671
NM_030662.3(MAP2K2):c.1093-6T>C	rs369681843
NM_030662.3(MAP2K2):c.1162C>T (p.Arg388Trp)	rs144383241
NM_030662.3(MAP2K2):c.1194C>T (p.Thr398=)	rs144850779
NM_030662.3(MAP2K2):c.192C>T (p.Val64=)	rs8157
NM_030662.3(MAP2K2):c.240G>A (p.Ala80=)	rs543217722
NM_030662.3(MAP2K2):c.303+127A>G
NM_030662.3(MAP2K2):c.303+8C>G	rs199612401
NM_030662.3(MAP2K2):c.405G>C (p.Gly135=)	rs10424722
NM_030662.3(MAP2K2):c.420C>T (p.Asp140=)	rs369925884
NM_030662.3(MAP2K2):c.450+99A>G
NM_030662.3(MAP2K2):c.528+237T>C
NM_030662.3(MAP2K2):c.528+242T>G
NM_030662.3(MAP2K2):c.529-138G>A
NM_030662.3(MAP2K2):c.690G>A (p.Thr230=)	rs201287884
NM_030662.3(MAP2K2):c.705+179T>C
NM_030662.3(MAP2K2):c.813C>T (p.Asp271=)	rs201726622
NM_030662.3(MAP2K2):c.825G>A (p.Leu275=)	rs587781027
NM_030662.3(MAP2K2):c.844C>T (p.Pro282Ser)	rs142307980
NM_030662.3(MAP2K2):c.846C>T (p.Pro282=)	rs11539506
NM_030662.3(MAP2K2):c.893C>T (p.Pro298Leu)	rs200371894
NM_030662.3(MAP2K2):c.919+252C>T
NM_030662.3(MAP2K2):c.92+212_92+237delGGGAGGACGGGGCAGGGGGCCCTCGG
NM_030662.3(MAP2K2):c.981C>T (p.Asn327=)	rs143275018
NM_030662.3(MAP2K2):c.985-150C>G

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