ClinVar Miner

List of variants in gene NRAS reported as likely benign for Noonan syndrome and Noonan-related syndrome

Included ClinVar conditions (67):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_002524.4(NRAS):c.-208T>A rs2273267 0.01703
NM_002524.5(NRAS):c.*416A>C rs9724643 0.01360
NM_002524.5(NRAS):c.*3499C>T rs147926293 0.00568
NM_002524.5(NRAS):c.*3366G>T rs72994440 0.00380
NM_002524.5(NRAS):c.*3219C>G rs72994441 0.00379
NM_002524.5(NRAS):c.*2517A>G rs554048037 0.00142
NM_002524.5(NRAS):c.*3306A>G rs189738278 0.00124
NM_002524.5(NRAS):c.225C>T (p.Gly75=) rs142739534 0.00109
NM_002524.5(NRAS):c.*2464A>G rs140878667 0.00041
NM_002524.5(NRAS):c.360G>A (p.Leu120=) rs143020946 0.00034
NM_002524.5(NRAS):c.112-8A>G rs9724626 0.00024
NM_002524.5(NRAS):c.*2784T>A rs374889066 0.00021
NM_002524.5(NRAS):c.*583T>G rs555171083 0.00021
NM_002524.5(NRAS):c.*2816T>C rs370262800 0.00011
NM_002524.5(NRAS):c.*2327C>T rs533027827 0.00008
NM_002524.5(NRAS):c.*3500G>A rs528970050 0.00005
NM_002524.5(NRAS):c.36T>G (p.Gly12=) rs759764705 0.00005
NM_002524.5(NRAS):c.553C>T (p.Pro185Ser) rs374061873 0.00003
NM_002524.5(NRAS):c.*2510_*2515del rs549171175
NM_002524.5(NRAS):c.*2965del rs61652108
NM_002524.5(NRAS):c.443C>T (p.Thr148Ile) rs2101738617

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