ClinVar Miner

List of variants in gene FKTN reported as benign for congenital vitreoretinal dysplasia

Included ClinVar conditions (42):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_001079802.2(FKTN):c.*1133A>G rs2768282
NM_001079802.2(FKTN):c.*1638A>G
NM_001079802.2(FKTN):c.*1843A>T
NM_001079802.2(FKTN):c.*2280T>C rs1024366
NM_001079802.2(FKTN):c.*2298C>G
NM_001079802.2(FKTN):c.*3778T>C
NM_001079802.2(FKTN):c.*5041G>A rs1854124
NM_001079802.2(FKTN):c.*5062G>A rs1854125
NM_001079802.2(FKTN):c.*5260G>T rs2010861
NM_001079802.2(FKTN):c.*5517T>C rs114655654
NM_001079802.2(FKTN):c.*5618T>A rs1048215
NM_001079802.2(FKTN):c.*786T>G rs10978177
NM_001079802.2(FKTN):c.*806G>C
NM_001079802.2(FKTN):c.-45G>T rs77013649
NM_001079802.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_001079802.2(FKTN):c.1026C>A (p.Leu342=) rs17309806
NM_001079802.2(FKTN):c.1336A>G (p.Asn446Asp) rs41313301
NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys) rs41277797
NM_001079802.2(FKTN):c.373G>A (p.Gly125Ser) rs34006675
NM_001079802.2(FKTN):c.42G>A (p.Thr14=) rs78794935
NM_001079802.2(FKTN):c.608G>A (p.Arg203Gln) rs34787999
NM_001079802.2(FKTN):c.668C>T (p.Thr223Ile) rs116105846
NM_006731.2(FKTN):c.106-10G>A rs148384394
NM_006731.2(FKTN):c.166-4A>G rs193922689
NM_006731.2(FKTN):c.166-6A>G rs41277795

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