ClinVar Miner

List of variants in gene LETM1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_012318.3(LETM1):c.804C>T (p.Ile268=) rs144059275 0.00082
NM_012318.3(LETM1):c.1044T>C (p.Leu348=) rs149533538 0.00062
NM_012318.3(LETM1):c.1467G>A (p.Ser489=) rs143000748 0.00043
NM_012318.3(LETM1):c.51C>T (p.Leu17=) rs1185311864 0.00035
NM_012318.3(LETM1):c.411C>T (p.Gly137=) rs148115434 0.00023
NM_012318.3(LETM1):c.843C>T (p.Ser281=) rs146247493 0.00023
NM_012318.3(LETM1):c.1521G>A (p.Pro507=) rs146433419 0.00021
NM_012318.3(LETM1):c.486G>A (p.Lys162=) rs147940094 0.00021
NM_012318.3(LETM1):c.53C>G (p.Pro18Arg) rs769399334 0.00021
NM_012318.3(LETM1):c.1917C>T (p.Asn639=) rs753632622 0.00011
NM_012318.3(LETM1):c.1992C>T (p.Pro664=) rs767887133 0.00010
NM_012318.3(LETM1):c.1476+7G>A rs367656668 0.00009
NM_012318.3(LETM1):c.1290C>T (p.Ala430=) rs199973293 0.00007
NM_012318.3(LETM1):c.82+12G>C rs906775342 0.00007
NM_012318.3(LETM1):c.1938C>T (p.Asn646=) rs138176193 0.00006
NM_012318.3(LETM1):c.1359C>T (p.Ala453=) rs141666504 0.00005
NM_012318.3(LETM1):c.1527C>T (p.Thr509=) rs199795241 0.00005
NM_012318.3(LETM1):c.1051C>A (p.Arg351=) rs746663018 0.00004
NM_012318.3(LETM1):c.1635C>T (p.Ile545=) rs374644730 0.00004
NM_012318.3(LETM1):c.1647C>T (p.Ser549=) rs772990450 0.00004
NM_012318.3(LETM1):c.1740C>T (p.Ser580=) rs779132484 0.00004
NM_012318.3(LETM1):c.2139A>G (p.Thr713=) rs755445723 0.00004
NM_012318.3(LETM1):c.855C>T (p.Asp285=) rs141242225 0.00004
NM_012318.3(LETM1):c.888A>G (p.Thr296=) rs776760287 0.00004
NM_012318.3(LETM1):c.948G>A (p.Leu316=) rs370730904 0.00004
NM_012318.3(LETM1):c.1608+8G>C rs767266602 0.00003
NM_012318.3(LETM1):c.1744-4T>C rs530212467 0.00003
NM_012318.3(LETM1):c.258G>A (p.Ala86=) rs746406341 0.00003
NM_012318.3(LETM1):c.477C>T (p.Asp159=) rs368052273 0.00002
NM_012318.3(LETM1):c.738+15C>T rs187369080 0.00002
NM_012318.3(LETM1):c.1200+17C>T rs201713811 0.00001
NM_012318.3(LETM1):c.1333-19G>C rs762995542 0.00001
NM_012318.3(LETM1):c.1350G>A (p.Val450=) rs761201580 0.00001
NM_012318.3(LETM1):c.1407G>A (p.Thr469=) rs779899501 0.00001
NM_012318.3(LETM1):c.1500G>C (p.Val500=) rs767063439 0.00001
NM_012318.3(LETM1):c.1728G>T (p.Val576=) rs746301139 0.00001
NM_012318.3(LETM1):c.2127G>A (p.Glu709=) rs748250467 0.00001
NM_012318.3(LETM1):c.2163G>A (p.Glu721=) rs780777776 0.00001
NM_012318.3(LETM1):c.282T>C (p.Gly94=) rs1451117627 0.00001
NM_012318.3(LETM1):c.333G>A (p.Ser111=) rs754403408 0.00001
NM_012318.3(LETM1):c.354G>A (p.Ser118=) rs759752511 0.00001
NM_012318.3(LETM1):c.441G>C (p.Val147=) rs944925756 0.00001
NM_012318.3(LETM1):c.83-16C>T rs750528895 0.00001
NM_012318.3(LETM1):c.999G>A (p.Leu333=) rs757215236 0.00001
NM_012318.3(LETM1):c.1003C>T (p.Leu335=) rs2108846315
NM_012318.3(LETM1):c.1029C>T (p.Phe343=) rs779708182
NM_012318.3(LETM1):c.1080+13A>G
NM_012318.3(LETM1):c.1110G>C (p.Leu370=)
NM_012318.3(LETM1):c.1134G>A (p.Ala378=)
NM_012318.3(LETM1):c.1164C>T (p.Gly388=)
NM_012318.3(LETM1):c.1173A>G (p.Glu391=)
NM_012318.3(LETM1):c.1182G>A (p.Leu394=)
NM_012318.3(LETM1):c.1200+9_1200+33del rs546855814
NM_012318.3(LETM1):c.1201-17C>T
NM_012318.3(LETM1):c.1230C>A (p.Ile410=)
NM_012318.3(LETM1):c.1245C>T (p.Leu415=)
NM_012318.3(LETM1):c.1272G>A (p.Pro424=)
NM_012318.3(LETM1):c.1293C>T (p.Asp431=)
NM_012318.3(LETM1):c.1332+18C>T
NM_012318.3(LETM1):c.1333-12C>A
NM_012318.3(LETM1):c.1333-9C>T
NM_012318.3(LETM1):c.1422G>A (p.Ala474=)
NM_012318.3(LETM1):c.143+16T>G
NM_012318.3(LETM1):c.143+18A>C
NM_012318.3(LETM1):c.144-9dup rs775068920
NM_012318.3(LETM1):c.1476+20C>T
NM_012318.3(LETM1):c.1477-15C>T
NM_012318.3(LETM1):c.1590G>A (p.Pro530=)
NM_012318.3(LETM1):c.1623G>A (p.Thr541=)
NM_012318.3(LETM1):c.165C>T (p.Cys55=)
NM_012318.3(LETM1):c.1744-13A>G
NM_012318.3(LETM1):c.1744-18C>G
NM_012318.3(LETM1):c.1822T>C (p.Leu608=)
NM_012318.3(LETM1):c.1833G>A (p.Arg611=)
NM_012318.3(LETM1):c.1864T>C (p.Leu622=)
NM_012318.3(LETM1):c.1931+14T>G
NM_012318.3(LETM1):c.1931+19G>A
NM_012318.3(LETM1):c.1931+7G>C rs1577308404
NM_012318.3(LETM1):c.1931+9G>A
NM_012318.3(LETM1):c.1932-19G>A
NM_012318.3(LETM1):c.1950C>T (p.Val650=)
NM_012318.3(LETM1):c.1956G>A (p.Glu652=) rs535845172
NM_012318.3(LETM1):c.1962C>A (p.Ile654=)
NM_012318.3(LETM1):c.1974G>A (p.Lys658=)
NM_012318.3(LETM1):c.2071-15T>C
NM_012318.3(LETM1):c.210C>T (p.Leu70=)
NM_012318.3(LETM1):c.211G>A (p.Gly71Ser)
NM_012318.3(LETM1):c.2202C>A (p.Val734=)
NM_012318.3(LETM1):c.2202C>T (p.Val734=)
NM_012318.3(LETM1):c.228G>A (p.Arg76=)
NM_012318.3(LETM1):c.251C>G (p.Ser84Trp) rs202034038
NM_012318.3(LETM1):c.279G>A (p.Val93=)
NM_012318.3(LETM1):c.351C>T (p.Asp117=)
NM_012318.3(LETM1):c.414C>G (p.Gly138=)
NM_012318.3(LETM1):c.417G>A (p.Pro139=)
NM_012318.3(LETM1):c.423C>T (p.Tyr141=)
NM_012318.3(LETM1):c.426C>T (p.Ser142=)
NM_012318.3(LETM1):c.432C>G (p.Pro144=) rs773611754
NM_012318.3(LETM1):c.432C>T (p.Pro144=) rs773611754
NM_012318.3(LETM1):c.466C>T (p.Arg156Trp)
NM_012318.3(LETM1):c.525C>G (p.Thr175=)
NM_012318.3(LETM1):c.657G>A (p.Pro219=)
NM_012318.3(LETM1):c.711A>G (p.Pro237=) rs2108848546
NM_012318.3(LETM1):c.732A>C (p.Ser244=)
NM_012318.3(LETM1):c.777G>A (p.Glu259=)
NM_012318.3(LETM1):c.83-13G>A
NM_012318.3(LETM1):c.876+11dup
NM_012318.3(LETM1):c.877-5C>G rs754669789
NM_012318.3(LETM1):c.933A>G (p.Leu311=)
NM_012318.3(LETM1):c.972G>A (p.Pro324=)

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