ClinVar Miner

List of variants in gene MAP2K1 reported as likely benign for not provided

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_002755.3(MAP2K1):c.-547C>T rs77540803 0.02251
NM_002755.4(MAP2K1):c.438+192C>T rs16949944 0.01566
NM_002755.4(MAP2K1):c.517-139G>T rs138624109 0.01336
NM_002755.4(MAP2K1):c.711G>A (p.Gly237=) rs17586159 0.01226
NM_002755.4(MAP2K1):c.516+283G>A rs192620467 0.00877
NM_002755.4(MAP2K1):c.693+234C>A rs142760272 0.00738
NM_002755.4(MAP2K1):c.517-230A>C rs141721809 0.00672
NM_002755.4(MAP2K1):c.439-168G>A rs187650018 0.00463
NM_002755.4(MAP2K1):c.1023-201del rs149355772 0.00405
NM_002755.4(MAP2K1):c.568+198C>T rs116786504 0.00354
NM_002755.4(MAP2K1):c.896-283G>A rs189306997 0.00344
NM_002755.4(MAP2K1):c.516+176A>G rs148929309 0.00322
NM_002755.4(MAP2K1):c.960+297A>G rs565603514 0.00299
NM_002755.4(MAP2K1):c.315C>T (p.Pro105=) rs144166521 0.00061
NM_002755.4(MAP2K1):c.848C>T (p.Ala283Val) rs144080051 0.00029
NM_002755.4(MAP2K1):c.6C>T (p.Pro2=) rs377720622 0.00025
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=) rs148656020 0.00024
NM_002755.4(MAP2K1):c.895+42G>A rs200724966 0.00021
NM_002755.4(MAP2K1):c.726G>T (p.Val242=) rs373745627 0.00013
NM_002755.4(MAP2K1):c.439-19C>A rs766207567 0.00010
NM_002755.4(MAP2K1):c.292-3C>T rs55694358 0.00007
NM_002755.4(MAP2K1):c.264G>A (p.Lys88=) rs7494832 0.00006
NM_002755.4(MAP2K1):c.277G>A (p.Val93Ile) rs151207265 0.00006
NM_002755.4(MAP2K1):c.729G>A (p.Gln243=) rs772752167 0.00005
NM_002755.4(MAP2K1):c.957C>T (p.Asn319=) rs143019052 0.00005
NM_002755.4(MAP2K1):c.771G>A (p.Ala257=) rs767965126 0.00003
NM_002755.4(MAP2K1):c.1005A>G (p.Gln335=) rs1057520833 0.00002
NM_002755.4(MAP2K1):c.568+11A>T rs769848510 0.00002
NM_002755.4(MAP2K1):c.439-18T>C rs751155864 0.00001
NM_002755.4(MAP2K1):c.568+9T>C rs748379069 0.00001
NM_002755.4(MAP2K1):c.792T>G (p.Pro264=) rs764379969 0.00001
NM_002755.4(MAP2K1):c.834G>A (p.Gln278=) rs148151221 0.00001
NM_002755.4(MAP2K1):c.961C>T (p.Pro321Ser) rs771613524 0.00001
NM_002755.4(MAP2K1):c.1023-17G>C rs759861076
NM_002755.4(MAP2K1):c.156C>G (p.Ala52=) rs147489724
NM_002755.4(MAP2K1):c.187C>T (p.Leu63=)
NM_002755.4(MAP2K1):c.291+14_291+20delinsTCTCACCAATCACCA rs1064795401
NM_002755.4(MAP2K1):c.36C>T (p.Asn12=) rs2140511663
NM_002755.4(MAP2K1):c.438+8A>T rs550240942
NM_002755.4(MAP2K1):c.517-9T>A rs758986316
NM_002755.4(MAP2K1):c.537T>C (p.Tyr179=) rs1188803242
NM_002755.4(MAP2K1):c.568+14005G>A
NM_002755.4(MAP2K1):c.694-12TC[4] rs113913469
NM_002755.4(MAP2K1):c.694-148G>C rs73471746
NM_002755.4(MAP2K1):c.80+14G>A rs1057522314
NM_002755.4(MAP2K1):c.896-284dup rs144137205
NM_002755.4(MAP2K1):c.9G>A (p.Lys3=)

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