ClinVar Miner

List of variants in gene FGFRL1 reported as likely benign for not provided

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Gene type:
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Total variants: 124
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HGVS dbSNP gnomAD frequency
NM_001004356.3(FGFRL1):c.1481G>A (p.Gly494Asp) rs149625647 0.00071
NM_001004356.3(FGFRL1):c.948C>T (p.Asp316=) rs147385493 0.00069
NM_001004356.3(FGFRL1):c.578G>A (p.Arg193His) rs4647937 0.00061
NM_001004356.3(FGFRL1):c.1260G>A (p.Pro420=) rs201785648 0.00058
NM_001004356.3(FGFRL1):c.1383C>T (p.Gly461=) rs148505744 0.00038
NM_001004356.3(FGFRL1):c.980G>A (p.Arg327His) rs147980100 0.00034
NM_001004356.3(FGFRL1):c.719-20C>T rs183356176 0.00026
NM_001004356.3(FGFRL1):c.1134C>T (p.Pro378=) rs111246053 0.00024
NM_001004356.3(FGFRL1):c.336C>T (p.Tyr112=) rs139057147 0.00021
NM_001004356.3(FGFRL1):c.1349A>G (p.His450Arg) rs182915641 0.00018
NM_001004356.3(FGFRL1):c.353-12G>A rs367793461 0.00015
NM_001004356.3(FGFRL1):c.291C>T (p.Tyr97=) rs113418020 0.00011
NM_001004356.3(FGFRL1):c.864C>T (p.Ala288=) rs138109269 0.00011
NM_001004356.3(FGFRL1):c.417C>T (p.Pro139=) rs376193356 0.00007
NM_001004356.3(FGFRL1):c.537G>T (p.Arg179=) rs768632874 0.00007
NM_001004356.3(FGFRL1):c.987C>T (p.Arg329=) rs368634271 0.00007
NM_001004356.3(FGFRL1):c.1257G>A (p.Pro419=) rs754631527 0.00005
NM_001004356.3(FGFRL1):c.1266G>A (p.Thr422=) rs375150331 0.00005
NM_001004356.3(FGFRL1):c.1020C>T (p.Gly340=) rs138509526 0.00004
NM_001004356.3(FGFRL1):c.309C>T (p.Asn103=) rs752971788 0.00004
NM_001004356.3(FGFRL1):c.780C>T (p.Phe260=) rs371754554 0.00004
NM_001004356.3(FGFRL1):c.876C>T (p.His292=) rs370405185 0.00004
NM_001004356.3(FGFRL1):c.894G>A (p.Val298=) rs781580876 0.00004
NM_001004356.3(FGFRL1):c.993C>T (p.Asp331=) rs757861533 0.00004
NM_001004356.3(FGFRL1):c.216C>T (p.Ser72=) rs372553975 0.00003
NM_001004356.3(FGFRL1):c.80-7C>T rs779324226 0.00003
NM_001004356.3(FGFRL1):c.858C>T (p.Tyr286=) rs769346621 0.00003
NM_001004356.3(FGFRL1):c.1233C>G (p.Ala411=) rs776053533 0.00002
NM_001004356.3(FGFRL1):c.433+17G>A rs756909908 0.00002
NM_001004356.3(FGFRL1):c.525C>T (p.Ser175=) rs1399378736 0.00002
NM_001004356.3(FGFRL1):c.1038C>T (p.Tyr346=) rs1312938489 0.00001
NM_001004356.3(FGFRL1):c.1059C>A (p.Leu353=) rs1343789800 0.00001
NM_001004356.3(FGFRL1):c.1434C>A (p.Ile478=) rs936127223 0.00001
NM_001004356.3(FGFRL1):c.315C>T (p.Phe105=) rs756531169 0.00001
NM_001004356.3(FGFRL1):c.480C>T (p.Ile160=) rs1283076647 0.00001
NM_001004356.3(FGFRL1):c.516C>T (p.Cys172=) rs779235733 0.00001
NM_001004356.3(FGFRL1):c.616C>T (p.Leu206=) rs1461926222 0.00001
NM_001004356.3(FGFRL1):c.684C>T (p.Gly228=) rs771046121 0.00001
NM_001004356.3(FGFRL1):c.718+17G>A rs763437948 0.00001
NM_001004356.3(FGFRL1):c.80-9C>T rs771445990 0.00001
NM_001004356.3(FGFRL1):c.873C>T (p.Arg291=) rs767391975 0.00001
NM_001004356.3(FGFRL1):c.1072+15C>T
NM_001004356.3(FGFRL1):c.1072+20C>T
NM_001004356.3(FGFRL1):c.1073-10G>A rs769826783
NM_001004356.3(FGFRL1):c.1073-11C>T
NM_001004356.3(FGFRL1):c.113G>A (p.Arg38Gln)
NM_001004356.3(FGFRL1):c.1143C>T (p.Ile381=) rs146112374
NM_001004356.3(FGFRL1):c.114G>A (p.Arg38=)
NM_001004356.3(FGFRL1):c.1155C>T (p.Ala385=) rs140148549
NM_001004356.3(FGFRL1):c.1158C>T (p.Gly386=)
NM_001004356.3(FGFRL1):c.1176C>G (p.Gly392=)
NM_001004356.3(FGFRL1):c.1215G>A (p.Pro405=)
NM_001004356.3(FGFRL1):c.1224C>T (p.Pro408=)
NM_001004356.3(FGFRL1):c.1263G>C (p.Gly421=) rs907710217
NM_001004356.3(FGFRL1):c.1272C>T (p.Arg424=)
NM_001004356.3(FGFRL1):c.1278C>T (p.Arg426=)
NM_001004356.3(FGFRL1):c.1302G>A (p.Ser434=) rs145786390
NM_001004356.3(FGFRL1):c.1302G>C (p.Ser434=) rs145786390
NM_001004356.3(FGFRL1):c.1317C>T (p.Ser439=)
NM_001004356.3(FGFRL1):c.1338G>A (p.Leu446=)
NM_001004356.3(FGFRL1):c.1347G>A (p.Glu449=) rs200350207
NM_001004356.3(FGFRL1):c.1359G>A (p.Pro453=)
NM_001004356.3(FGFRL1):c.1366C>T (p.Pro456Ser)
NM_001004356.3(FGFRL1):c.1378C>T (p.Leu460=)
NM_001004356.3(FGFRL1):c.1389C>G (p.Gly463=)
NM_001004356.3(FGFRL1):c.1391C>A (p.Pro464Gln) rs4647932
NM_001004356.3(FGFRL1):c.1431C>T (p.Asp477=)
NM_001004356.3(FGFRL1):c.1452_1455del (p.His485fs) rs145808953
NM_001004356.3(FGFRL1):c.1452_1455dup (p.Ser486fs) rs145808953
NM_001004356.3(FGFRL1):c.1497C>T (p.His499=)
NM_001004356.3(FGFRL1):c.171G>A (p.Pro57=)
NM_001004356.3(FGFRL1):c.178C>T (p.Leu60=) rs1577567162
NM_001004356.3(FGFRL1):c.192C>T (p.Thr64=) rs1326499468
NM_001004356.3(FGFRL1):c.22C>T (p.Leu8=) rs753833720
NM_001004356.3(FGFRL1):c.243G>A (p.Pro81=)
NM_001004356.3(FGFRL1):c.285C>A (p.Gly95=)
NM_001004356.3(FGFRL1):c.285C>T (p.Gly95=)
NM_001004356.3(FGFRL1):c.300G>A (p.Lys100=)
NM_001004356.3(FGFRL1):c.327C>T (p.Ser109=)
NM_001004356.3(FGFRL1):c.352+15C>T
NM_001004356.3(FGFRL1):c.352+16G>C rs4647934
NM_001004356.3(FGFRL1):c.352+16G>T
NM_001004356.3(FGFRL1):c.353-17C>T
NM_001004356.3(FGFRL1):c.353-19C>T
NM_001004356.3(FGFRL1):c.353-8C>G
NM_001004356.3(FGFRL1):c.379C>T (p.Leu127=)
NM_001004356.3(FGFRL1):c.393C>T (p.Ser131=)
NM_001004356.3(FGFRL1):c.399T>C (p.Ser133=)
NM_001004356.3(FGFRL1):c.40C>T (p.Leu14=)
NM_001004356.3(FGFRL1):c.433+7A>T rs1560564293
NM_001004356.3(FGFRL1):c.434-12C>T
NM_001004356.3(FGFRL1):c.434-17G>A
NM_001004356.3(FGFRL1):c.45G>C (p.Leu15=)
NM_001004356.3(FGFRL1):c.477G>C (p.Val159=)
NM_001004356.3(FGFRL1):c.489C>A (p.Pro163=) rs113814624
NM_001004356.3(FGFRL1):c.489C>T (p.Pro163=) rs113814624
NM_001004356.3(FGFRL1):c.504G>A (p.Val168=)
NM_001004356.3(FGFRL1):c.510C>T (p.Leu170=)
NM_001004356.3(FGFRL1):c.522C>G (p.Ala174=)
NM_001004356.3(FGFRL1):c.540C>T (p.Pro180=)
NM_001004356.3(FGFRL1):c.648C>T (p.Ser216=)
NM_001004356.3(FGFRL1):c.66C>T (p.Ala22=)
NM_001004356.3(FGFRL1):c.681G>A (p.Ala227=)
NM_001004356.3(FGFRL1):c.693C>T (p.Asn231=)
NM_001004356.3(FGFRL1):c.714G>A (p.Val238=)
NM_001004356.3(FGFRL1):c.714G>T (p.Val238=)
NM_001004356.3(FGFRL1):c.718+14C>T
NM_001004356.3(FGFRL1):c.718+16G>A
NM_001004356.3(FGFRL1):c.719-10G>A
NM_001004356.3(FGFRL1):c.719-11C>T
NM_001004356.3(FGFRL1):c.719-17G>T
NM_001004356.3(FGFRL1):c.719-7C>T rs1212728784
NM_001004356.3(FGFRL1):c.75C>T (p.Ala25=)
NM_001004356.3(FGFRL1):c.768G>A (p.Thr256=)
NM_001004356.3(FGFRL1):c.79+13G>T rs1715655800
NM_001004356.3(FGFRL1):c.79+20C>T
NM_001004356.3(FGFRL1):c.79+8C>A
NM_001004356.3(FGFRL1):c.897C>A (p.Gly299=)
NM_001004356.3(FGFRL1):c.897C>T (p.Gly299=)
NM_001004356.3(FGFRL1):c.945C>T (p.Pro315=)
NM_001004356.3(FGFRL1):c.960C>A (p.Leu320=)
NM_001004356.3(FGFRL1):c.96G>A (p.Ala32=)
NM_001004356.3(FGFRL1):c.990G>A (p.Gln330=)
NM_001004356.3(FGFRL1):c.996T>C (p.Asp332=)

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