ClinVar Miner

List of variants in gene ALK reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_004304.5(ALK):c.1464C>T (p.Gly488=) rs56165377 0.00615
NM_004304.5(ALK):c.1110G>A (p.Glu370=) rs138784554 0.00195
NM_004304.5(ALK):c.3594C>T (p.Leu1198=) rs56071005 0.00166
NM_004304.5(ALK):c.2676C>T (p.Ala892=) rs138668699 0.00164
NM_004304.5(ALK):c.2613C>T (p.Asn871=) rs150557024 0.00093
NM_004304.5(ALK):c.1755C>T (p.Ala585=) rs373605278 0.00032
NM_004304.5(ALK):c.2526C>T (p.Ala842=) rs145271283 0.00029
NM_004304.5(ALK):c.3633C>A (p.Thr1211=) rs144437923 0.00021
NM_004304.5(ALK):c.2478C>T (p.Tyr826=) rs142126984 0.00016
NM_004304.5(ALK):c.2229C>T (p.Gly743=) rs111253753 0.00015
NM_004304.5(ALK):c.597C>T (p.Gly199=) rs200868013 0.00012
NM_004304.5(ALK):c.4473G>A (p.Lys1491=) rs148987382 0.00007
NM_004304.5(ALK):c.1107C>T (p.Asn369=) rs114429299 0.00005
NM_004304.5(ALK):c.3453G>A (p.Thr1151=) rs145061595 0.00005
NM_004304.5(ALK):c.32C>T (p.Pro11Leu) rs767822322 0.00004
NM_004304.5(ALK):c.3645G>A (p.Pro1215=) rs775768862 0.00004
NM_004304.5(ALK):c.4656G>A (p.Gly1552=) rs952457982 0.00004
NM_004304.5(ALK):c.255C>T (p.Pro85=) rs372277804 0.00003
NM_004304.5(ALK):c.3849T>C (p.Tyr1283=) rs960416635 0.00003
NM_004304.5(ALK):c.4425C>T (p.His1475=) rs139039449 0.00003
NM_004304.5(ALK):c.924G>A (p.Gly308=) rs878854660 0.00002
NM_004304.5(ALK):c.2457A>G (p.Gly819=) rs147842434 0.00001
NM_004304.5(ALK):c.4752C>T (p.Tyr1584=) rs758556216 0.00001
NM_004304.5(ALK):c.1614G>A (p.Thr538=) rs374205057
NM_004304.5(ALK):c.3067+26A>G
NM_004304.5(ALK):c.3067+91G>A
NM_004304.5(ALK):c.3068-360_3068-357del
NM_004304.5(ALK):c.3068-43A>G
NM_004304.5(ALK):c.3240G>A (p.Leu1080=) rs760768939
NM_004304.5(ALK):c.3420C>T (p.Asn1140=) rs150785816
NM_004304.5(ALK):c.3600G>A (p.Ala1200=) rs56247462
NM_004304.5(ALK):c.3654C>T (p.Pro1218=)
NM_004304.5(ALK):c.4350C>T (p.Gly1450=)
NM_004304.5(ALK):c.66G>C (p.Gly22=) rs778418435
NM_004304.5(ALK):c.954C>G (p.Gly318=)

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