ClinVar Miner

List of variants in gene SRRM1 reported as uncertain significance

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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_005839.4(SRRM1):c.1952G>T (p.Arg651Ile) rs144308305 0.00073
NM_005839.4(SRRM1):c.1953A>C (p.Arg651Ser) rs141233962 0.00073
NM_005839.4(SRRM1):c.1709G>A (p.Arg570His) rs78787676 0.00027
NM_005839.4(SRRM1):c.2012G>A (p.Arg671Gln) rs533910355 0.00009
NM_005839.4(SRRM1):c.1601G>A (p.Arg534Gln) rs373180505 0.00007
NM_005839.4(SRRM1):c.523C>T (p.Arg175Cys) rs200425080 0.00007
NM_005839.4(SRRM1):c.2003G>A (p.Arg668His) rs147133886 0.00005
NM_005839.4(SRRM1):c.2344C>T (p.Pro782Ser) rs369635682 0.00004
NM_005839.4(SRRM1):c.2327C>T (p.Pro776Leu) rs150723178 0.00003
NM_005839.4(SRRM1):c.2374C>T (p.Pro792Ser) rs139728420 0.00003
NM_005839.4(SRRM1):c.866G>A (p.Arg289Gln) rs776382421 0.00003
NM_005839.4(SRRM1):c.1145C>T (p.Pro382Leu) rs766551832 0.00002
NM_005839.4(SRRM1):c.1898G>A (p.Arg633Gln) rs757498986 0.00002
NM_005839.4(SRRM1):c.1096C>T (p.Arg366Cys) rs774225218 0.00001
NM_005839.4(SRRM1):c.1675C>T (p.Arg559Trp) rs1439720845 0.00001
NM_005839.4(SRRM1):c.1736G>A (p.Arg579Gln) rs199920108 0.00001
NM_005839.4(SRRM1):c.1999A>G (p.Ser667Gly) rs565269582 0.00001
NM_005839.4(SRRM1):c.2276C>T (p.Pro759Leu) rs138138056 0.00001
NM_005839.4(SRRM1):c.2393C>T (p.Pro798Leu) rs777632895 0.00001
NM_005839.4(SRRM1):c.2420G>A (p.Gly807Asp) rs759803310 0.00001
NM_005839.4(SRRM1):c.842G>A (p.Arg281His) rs756779870 0.00001
NM_005839.4(SRRM1):c.1070G>C (p.Gly357Ala)
NM_005839.4(SRRM1):c.121A>T (p.Ser41Cys)
NM_005839.4(SRRM1):c.1241C>T (p.Ser414Phe) rs200765096
NM_005839.4(SRRM1):c.1268C>G (p.Thr423Arg)
NM_005839.4(SRRM1):c.1288G>C (p.Val430Leu) rs2523622951
NM_005839.4(SRRM1):c.1310G>C (p.Gly437Ala)
NM_005839.4(SRRM1):c.1412G>A (p.Gly471Asp)
NM_005839.4(SRRM1):c.1418T>C (p.Met473Thr)
NM_005839.4(SRRM1):c.1561C>T (p.Arg521Trp)
NM_005839.4(SRRM1):c.1619C>T (p.Thr540Ile) rs776543273
NM_005839.4(SRRM1):c.1621T>C (p.Ser541Pro)
NM_005839.4(SRRM1):c.1757C>T (p.Pro586Leu) rs139001382
NM_005839.4(SRRM1):c.1763G>A (p.Arg588Gln)
NM_005839.4(SRRM1):c.1766G>A (p.Arg589His)
NM_005839.4(SRRM1):c.1882T>C (p.Ser628Pro)
NM_005839.4(SRRM1):c.1886C>T (p.Pro629Leu) rs1671565970
NM_005839.4(SRRM1):c.1982G>A (p.Arg661Lys)
NM_005839.4(SRRM1):c.1991C>G (p.Ser664Cys)
NM_005839.4(SRRM1):c.2021G>A (p.Arg674Gln) rs376931789
NM_005839.4(SRRM1):c.2021G>C (p.Arg674Pro)
NM_005839.4(SRRM1):c.2098G>C (p.Val700Leu) rs142386020
NM_005839.4(SRRM1):c.2252G>A (p.Arg751Gln)
NM_005839.4(SRRM1):c.2252G>C (p.Arg751Pro) rs201082864
NM_005839.4(SRRM1):c.2332A>G (p.Thr778Ala) rs778334316
NM_005839.4(SRRM1):c.2347G>A (p.Ala783Thr)
NM_005839.4(SRRM1):c.2350G>C (p.Val784Leu)
NM_005839.4(SRRM1):c.2354C>T (p.Pro785Leu)
NM_005839.4(SRRM1):c.2375C>G (p.Pro792Arg)
NM_005839.4(SRRM1):c.2392C>T (p.Pro798Ser)
NM_005839.4(SRRM1):c.2509G>A (p.Val837Met) rs1378693672
NM_005839.4(SRRM1):c.430A>G (p.Met144Val)
NM_005839.4(SRRM1):c.440A>C (p.Gln147Pro)
NM_005839.4(SRRM1):c.46C>T (p.Arg16Trp)
NM_005839.4(SRRM1):c.496A>G (p.Arg166Gly)
NM_005839.4(SRRM1):c.517A>G (p.Arg173Gly) rs2523210181
NM_005839.4(SRRM1):c.623G>A (p.Arg208Gln)
NM_005839.4(SRRM1):c.628C>T (p.Pro210Ser)
NM_005839.4(SRRM1):c.673G>C (p.Glu225Gln)
NM_005839.4(SRRM1):c.704T>G (p.Val235Gly)
NM_005839.4(SRRM1):c.715A>G (p.Thr239Ala) rs1183876878
NM_005839.4(SRRM1):c.730A>T (p.Ile244Phe) rs377349401
NM_005839.4(SRRM1):c.775C>A (p.Pro259Thr) rs1241225555
NM_005839.4(SRRM1):c.871C>G (p.Arg291Gly) rs1009577703
NM_005839.4(SRRM1):c.872G>A (p.Arg291His) rs142015455
NM_005839.4(SRRM1):c.872G>C (p.Arg291Pro)
NM_005839.4(SRRM1):c.877C>T (p.Pro293Ser) rs1222679257
NM_005839.4(SRRM1):c.883C>T (p.His295Tyr)

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