ClinVar Miner

List of variants in gene FGFR2 reported as likely benign for not provided

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Total variants: 26
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HGVS dbSNP
NM_000141.5(FGFR2):c.1084+8C>T
NM_000141.5(FGFR2):c.1545C>T (p.Ala515=)
NM_000141.5(FGFR2):c.1561+7G>A
NM_000141.5(FGFR2):c.159G>T (p.Ala53=)
NM_000141.5(FGFR2):c.1911C>T (p.Asn637=)
NM_000141.5(FGFR2):c.1987-5T>G
NM_000141.5(FGFR2):c.2247G>A (p.Thr749=)
NM_000141.5(FGFR2):c.252G>A (p.Arg84=)
NM_000141.5(FGFR2):c.377-6A>T
NM_000141.5(FGFR2):c.390C>G (p.Ser130=)
NM_000141.5(FGFR2):c.714G>A (p.Gly238=)
NM_000141.5(FGFR2):c.780C>T (p.Ala260=)
NM_022970.3(FGFR2):c.110-54C>T
NM_022970.3(FGFR2):c.1242G>A (p.Pro414=) rs147674677
NM_022970.3(FGFR2):c.1443-231C>T
NM_022970.3(FGFR2):c.159G>A (p.Ala53=) rs1047102
NM_022970.3(FGFR2):c.170C>T (p.Ser57Leu) rs56226109
NM_022970.3(FGFR2):c.1821C>T (p.Cys607=) rs371395564
NM_022970.3(FGFR2):c.2061-10T>C
NM_022970.3(FGFR2):c.2109G>A (p.Ser703=) rs794727163
NM_022970.3(FGFR2):c.234C>T (p.His78=)
NM_022970.3(FGFR2):c.23T>G (p.Ile8Ser) rs147307031
NM_022970.3(FGFR2):c.34G>A (p.Val12Met) rs143978938
NM_022970.3(FGFR2):c.377-10T>C
NM_022970.3(FGFR2):c.625-10A>G rs201512833
NM_022970.3(FGFR2):c.759T>G (p.Pro253=) rs3135755

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