ClinVar Miner

List of variants studied for familial papillary or follicular thyroid carcinoma by OMIM

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_004473.4(FOXE1):c.743C>G (p.Ala248Gly) rs538912281 0.00247
NM_020762.4(SRGAP1):c.1849C>T (p.Arg617Cys) rs114817817 0.00101
NM_020762.4(SRGAP1):c.447A>C (p.Gln149His) rs781626187 0.00001
NM_002524.5(NRAS):c.182A>G (p.Gln61Arg) rs11554290
NM_004333.6(BRAF):c.1801A>G (p.Lys601Glu) rs121913364
NM_004897.5(MINPP1):c.122C>T (p.Ser41Leu) rs119486096
NM_004897.5(MINPP1):c.809A>G (p.Gln270Arg) rs104894171
NM_005343.4(HRAS):c.181C>A (p.Gln61Lys) rs28933406
NM_020762.4(SRGAP1):c.823G>A (p.Ala275Thr) rs797044990

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