"PreventionGenetics, part of Exact Sciences"[submitter] AND "FOXD1"[ge - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056416	NM_004472.3(FOXD1):c.1290_1295dup (p.Ala434_Ser435insAlaAla)	FOXD1	Duplication (inframe insertion)	FOXD1-related disorder	GLikely benign
Select item 3029284	NM_004472.3(FOXD1):c.1260C>T (p.Ala420=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3052425	NM_004472.3(FOXD1):c.1251C>A (p.Gly417=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3029712	NM_004472.3(FOXD1):c.1170CTCGCC[4] (p.Pro396_Val397insSerPro)	FOXD1	Microsatellite (inframe insertion)	FOXD1-related disorder	GLikely benign
Select item 3042166	NM_004472.3(FOXD1):c.1146_1160del (p.Gln383_Ala387del)	FOXD1	Deletion (inframe deletion)	FOXD1-related disorder	GBenign
Select item 2602786	NM_004472.3(FOXD1):c.1005C>T (p.Gly335=)	FOXD1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 3037543	NM_004472.3(FOXD1):c.889_890dup (p.Ala298fs)	FOXD1 (A298fs)	Duplication (frameshift variant)	FOXD1-related disorder	GLikely benign
Select item 3029354	NM_004472.3(FOXD1):c.858G>A (p.Ala286=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3056830	NM_004472.3(FOXD1):c.798G>A (p.Pro266=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3052761	NM_004472.3(FOXD1):c.789G>C (p.Pro263=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3037053	NM_004472.3(FOXD1):c.759C>G (p.Ala253=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3036957	NM_004472.3(FOXD1):c.756A>G (p.Ala252=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3032563	NM_004472.3(FOXD1):c.744G>T (p.Ala248=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3039829	NM_004472.3(FOXD1):c.681C>A (p.Leu227=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3037186	NM_004472.3(FOXD1):c.612G>A (p.Glu204=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3030145	NM_004472.3(FOXD1):c.609G>C (p.Pro203=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3030811	NM_004472.3(FOXD1):c.564C>G (p.Arg188=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3047224	NM_004472.3(FOXD1):c.486C>T (p.Tyr162=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3034442	NM_004472.3(FOXD1):c.318_338del (p.Gly107_Gly113del)	FOXD1	Deletion (inframe deletion)	FOXD1-related disorder	GLikely benign
Select item 3047045	NM_004472.3(FOXD1):c.333C>A (p.Gly111=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3051510	NM_004472.3(FOXD1):c.324C>G (p.Gly108=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3054868	NM_004472.3(FOXD1):c.315C>T (p.Gly105=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3039406	NM_004472.3(FOXD1):c.273C>G (p.Gly91=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3056198	NM_004472.3(FOXD1):c.263C>G (p.Ala88Gly)	FOXD1 (A88G)	Single nucleotide variant (missense variant)	FOXD1-related disorder	GBenign
Select item 3045741	NM_004472.3(FOXD1):c.255C>T (p.Gly85=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3037294	NM_004472.3(FOXD1):c.237G>A (p.Leu79=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3055836	NM_004472.3(FOXD1):c.153GCG[5] (p.Arg57del)	FOXD1 (R57del)	Microsatellite (inframe deletion)	FOXD1-related disorder	GBenign
Select item 3045411	NM_004472.3(FOXD1):c.6C>T (p.Thr2=)	FOXD1	Single nucleotide variant (synonymous variant)	FOXD1-related disorder	GLikely benign
Select item 3036775	NM_004472.3(FOXD1):c.-6A>C	FOXD1	Single nucleotide variant (5 prime UTR variant)	FOXD1-related disorder	GLikely benign
Select item 3038294	NM_004472.3(FOXD1):c.-21CGC[3]	FOXD1	Microsatellite (5 prime UTR variant)	FOXD1-related disorder	GLikely benign

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Items: 30