Related gene-specific medical variations for Gene (Select 26032) - ClinVar

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Links from Gene

Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323696	NM_015551.2(SUSD5):c.1463A>G (p.Tyr488Cys)	LOC126806648, SUSD5 (Y488C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323695	NM_015551.2(SUSD5):c.1352C>T (p.Pro451Leu)	LOC126806648, SUSD5 (P451L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323694	NM_015551.2(SUSD5):c.1403A>G (p.Tyr468Cys)	LOC126806648, SUSD5 (Y468C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3234363	NM_015551.2(SUSD5):c.723T>A (p.Ser241=)	LOC126806648, SUSD5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3172306	NM_015551.2(SUSD5):c.999A>T (p.Glu333Asp)	LOC126806648, SUSD5 (E333D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172303	NM_015551.2(SUSD5):c.1727T>G (p.Ile576Ser)	LOC126806648, SUSD5 (I576S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172302	NM_015551.2(SUSD5):c.1642G>A (p.Gly548Arg)	LOC126806648, SUSD5 (G548R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172300	NM_015551.2(SUSD5):c.1538C>T (p.Thr513Met)	LOC126806648, SUSD5 (T513M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172299	NM_015551.2(SUSD5):c.1379T>C (p.Ile460Thr)	LOC126806648, SUSD5 (I460T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172297	NM_015551.2(SUSD5):c.1330G>T (p.Val444Leu)	LOC126806648, SUSD5 (V444L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3172296	NM_015551.2(SUSD5):c.1031A>G (p.Asp344Gly)	LOC126806648, SUSD5 (D344G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614646	NM_015551.2(SUSD5):c.1210A>C (p.Asn404His)	LOC126806648, SUSD5 (N404H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603941	NM_015551.2(SUSD5):c.1248A>C (p.Glu416Asp)	LOC126806648, SUSD5 (E416D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543276	NM_015551.2(SUSD5):c.1186G>A (p.Asp396Asn)	LOC126806648, SUSD5 (D396N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531056	NM_015551.2(SUSD5):c.1624T>C (p.Phe542Leu)	LOC126806648, SUSD5 (F542L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2523832	NM_015551.2(SUSD5):c.1469T>C (p.Leu490Pro)	LOC126806648, SUSD5 (L490P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454394	NM_015551.2(SUSD5):c.1545G>C (p.Met515Ile)	LOC126806648, SUSD5 (M515I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406543	NM_015551.2(SUSD5):c.1021G>A (p.Gly341Ser)	LOC126806648, SUSD5 (G341S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2405783	NM_015551.2(SUSD5):c.1694A>G (p.Asp565Gly)	LOC126806648, SUSD5 (D565G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2392425	NM_015551.2(SUSD5):c.1696G>A (p.Gly566Arg)	LOC126806648, SUSD5 (G566R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380070	NM_015551.2(SUSD5):c.911C>T (p.Pro304Leu)	LOC126806648, SUSD5 (P304L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377135	NM_015551.2(SUSD5):c.745C>A (p.Arg249Ser)	LOC126806648, SUSD5 (R249S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342599	NM_015551.2(SUSD5):c.1573A>G (p.Thr525Ala)	LOC126806648, SUSD5 (T525A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258213	NM_015551.2(SUSD5):c.1784T>C (p.Val595Ala)	LOC126806648, SUSD5 (V595A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243059	NM_015551.2(SUSD5):c.1232A>G (p.Gln411Arg)	LOC126806648, SUSD5 (Q411R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216530	NM_015551.2(SUSD5):c.1467G>T (p.Glu489Asp)	LOC126806648, SUSD5 (E489D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212524	NM_015551.2(SUSD5):c.1367A>G (p.Glu456Gly)	LOC126806648, SUSD5 (E456G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209361	NM_015551.2(SUSD5):c.1286A>G (p.Glu429Gly)	LOC126806648, SUSD5 (E429G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 28