Related gene-specific medical variations for Gene (Select 85453) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329688	NM_033512.3(TSPYL5):c.575G>T (p.Gly192Val)	LOC101927066, TSPYL5 (G192V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3329687	NM_033512.3(TSPYL5):c.814G>C (p.Glu272Gln)	LOC101927066, TSPYL5 (E272Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3329686	NM_033512.3(TSPYL5):c.517G>T (p.Ala173Ser)	LOC101927066, TSPYL5 (A173S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3329685	NM_033512.3(TSPYL5):c.1020C>A (p.Ser340Arg)	LOC101927066, TSPYL5 (S340R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183909	NM_033512.3(TSPYL5):c.760C>A (p.Gln254Lys)	LOC101927066, TSPYL5 (Q254K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183908	NM_033512.3(TSPYL5):c.686A>G (p.Lys229Arg)	LOC101927066, TSPYL5 (K229R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183907	NM_033512.3(TSPYL5):c.602G>A (p.Ser201Asn)	LOC101927066, TSPYL5 (S201N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183906	NM_033512.3(TSPYL5):c.440A>G (p.Lys147Arg)	LOC101927066, TSPYL5 (K147R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183905	NM_033512.3(TSPYL5):c.32C>T (p.Ser11Phe)	LOC101927066, TSPYL5 (S11F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3183904	NM_033512.3(TSPYL5):c.1156G>A (p.Gly386Arg)	LOC101927066, TSPYL5 (G386R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658701	NM_033512.3(TSPYL5):c.819A>G (p.Val273=)	LOC101927066, TSPYL5	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2557160	NM_033512.3(TSPYL5):c.1162C>T (p.Arg388Cys)	LOC101927066, TSPYL5 (R388C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478390	NM_033512.3(TSPYL5):c.214C>T (p.Arg72Trp)	LOC101927066, TSPYL5 (R72W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470664	NM_033512.3(TSPYL5):c.977C>T (p.Thr326Ile)	LOC101927066, TSPYL5 (T326I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359550	NM_033512.3(TSPYL5):c.1042C>T (p.Arg348Cys)	LOC101927066, TSPYL5 (R348C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342507	NM_033512.3(TSPYL5):c.505A>G (p.Lys169Glu)	LOC101927066, TSPYL5 (K169E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318715	NM_033512.3(TSPYL5):c.449C>G (p.Pro150Arg)	LOC101927066, TSPYL5 (P150R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296325	NM_033512.3(TSPYL5):c.1237G>A (p.Val413Met)	LOC101927066, TSPYL5 (V413M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290385	NM_033512.3(TSPYL5):c.593C>T (p.Thr198Met)	LOC101927066, TSPYL5 (T198M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288927	NM_033512.3(TSPYL5):c.741T>G (p.Asn247Lys)	LOC101927066, TSPYL5 (N247K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260502	NM_033512.3(TSPYL5):c.436G>C (p.Gly146Arg)	LOC101927066, TSPYL5 (G146R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250117	NM_033512.3(TSPYL5):c.409C>G (p.Arg137Gly)	LOC101927066, TSPYL5 (R137G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233311	NM_033512.3(TSPYL5):c.67G>C (p.Ala23Pro)	LOC101927066, TSPYL5 (A23P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213614	NM_033512.3(TSPYL5):c.220G>A (p.Gly74Arg)	LOC101927066, TSPYL5 (G74R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783011	NM_033512.3(TSPYL5):c.407C>T (p.Pro136Leu)	LOC101927066, TSPYL5 (P136L)	Single nucleotide variant (missense variant)	not provided	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 25