"Genetic Services Laboratory, University of Chicago"[submitter] AND "F - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 391893	NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu)	FAT4 (R175L)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 388443	NM_001291303.3(FAT4):c.2811G>T (p.Lys937Asn)	FAT4 (K937N)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 384625	NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser)	FAT4 (L1385S)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 377854	NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val)	FAT4 (I1435V)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 376888	NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)	FAT4 (I1759V)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 2443132	NM_001291303.3(FAT4):c.5322C>T (p.Leu1774=)	FAT4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 435175	NM_001291303.3(FAT4):c.5987A>G (p.Lys1996Arg)	FAT4 (K1996R)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 435176	NM_001291303.3(FAT4):c.7358G>T (p.Ser2453Ile)	FAT4 (S2451I +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +3 more	GBenign/Likely benign
Select item 1167898	NM_001291303.3(FAT4):c.7466C>T (p.Ala2489Val)	FAT4 (A2487V +1 more)	Single nucleotide variant (missense variant)	FAT4-related disorder +2 more	GBenign/Likely benign
Select item 517910	NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val)	FAT4 (I2603V +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1337802	NM_001291303.3(FAT4):c.7848T>G (p.Ile2616Met)	FAT4 (I2614M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 435173	NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GBenign/Likely benign
Select item 429367	NM_001291303.3(FAT4):c.8078C>T (p.Ser2693Leu)	FAT4 (S2691L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1337702	NM_001291303.3(FAT4):c.8332A>C (p.Ile2778Leu)	FAT4 (I2776L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1337703	NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu)	FAT4 (D3197E +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 435174	NM_001291303.3(FAT4):c.9696G>A (p.Ala3232=)	FAT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 384299	NM_001291303.3(FAT4):c.9891G>A (p.Val3297=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1336624	NM_001291303.3(FAT4):c.10155T>A (p.Gly3385=)	FAT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 252740	NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met)	FAT4 (T3616M +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 380887	NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp)	FAT4 (R4022W +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 787977	NM_001291303.3(FAT4):c.12479+8G>A	FAT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 380888	NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=)	FAT4	Single nucleotide variant (synonymous variant)	FAT4-related disorder +2 more	GBenign/Likely benign
Select item 388998	NM_001291303.3(FAT4):c.12986A>G (p.Asp4329Gly)	FAT4 (D4327G +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 381278	NM_001291303.3(FAT4):c.13605G>A (p.Lys4535=)	FAT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1336717	NM_001291303.3(FAT4):c.14726C>T (p.Ala4909Val)	FAT4 (A4907V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25