ClinVar Miner

List of variants in gene ERBB2 reported as uncertain significance for Glioma susceptibility 1; Ovarian cancer; Gastric cancer; Lung cancer; Visceral neuropathy, familial, 2, autosomal recessive

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_004448.4(ERBB2):c.1466C>T (p.Pro489Leu) rs142456637 0.00069
NM_004448.4(ERBB2):c.455G>C (p.Gly152Ala) rs151122410 0.00036
NM_004448.4(ERBB2):c.1179G>A (p.Gln393=) rs147204600 0.00018
NM_004448.4(ERBB2):c.649C>T (p.Arg217Cys) rs768151310 0.00009
NM_004448.4(ERBB2):c.3142C>T (p.Arg1048Cys) rs377602610 0.00008
NM_004448.4(ERBB2):c.3166G>A (p.Gly1056Ser) rs574436396 0.00007
NM_004448.4(ERBB2):c.1793C>A (p.Ala598Asp) rs145409713 0.00004
NM_004448.4(ERBB2):c.734C>T (p.Thr245Met) rs376183465 0.00004
NM_004448.4(ERBB2):c.74T>C (p.Val25Ala) rs755921683 0.00004
NM_004448.4(ERBB2):c.1409A>G (p.His470Arg) rs201097345 0.00002
NM_004448.4(ERBB2):c.608G>A (p.Arg203His) rs896171398 0.00002
NM_004448.4(ERBB2):c.1772A>T (p.Lys591Met) rs767216520 0.00001
NM_004448.4(ERBB2):c.199A>G (p.Thr67Ala) rs778575008 0.00001
NM_004448.4(ERBB2):c.1195G>A (p.Val399Met)
NM_004448.4(ERBB2):c.1270G>A (p.Val424Ile)
NM_004448.4(ERBB2):c.1314-3T>C
NM_004448.4(ERBB2):c.1506C>A (p.Asp502Glu)
NM_004448.4(ERBB2):c.1513+17A>G
NM_004448.4(ERBB2):c.1550G>A (p.Arg517Gln)
NM_004448.4(ERBB2):c.1556A>G (p.His519Arg)
NM_004448.4(ERBB2):c.1894C>T (p.His632Tyr)
NM_004448.4(ERBB2):c.2085+7C>T
NM_004448.4(ERBB2):c.2458C>G (p.Gln820Glu)
NM_004448.4(ERBB2):c.2726del
NM_004448.4(ERBB2):c.2835_2836insT (p.Ile946fs)
NM_004448.4(ERBB2):c.3019T>A (p.Ser1007Thr)
NM_004448.4(ERBB2):c.3110C>T (p.Pro1037Leu)
NM_004448.4(ERBB2):c.3288G>C (p.Lys1096Asn)
NM_004448.4(ERBB2):c.3463G>T (p.Gly1155Cys)
NM_004448.4(ERBB2):c.3573G>A (p.Val1191=)
NM_004448.4(ERBB2):c.562C>T (p.Arg188Cys)
NM_004448.4(ERBB2):c.569G>A (p.Arg190Gln)
NM_004448.4(ERBB2):c.647C>T (p.Thr216Met)
NM_004448.4(ERBB2):c.655G>C (p.Val219Leu)
NM_004448.4(ERBB2):c.818C>T (p.Thr273Ile)

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