TEX26[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2272578	NM_152325.3(TEX26):c.16C>A (p.Pro6Thr)	TEX26 (P6T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2643713	NM_152325.3(TEX26):c.39C>T (p.Leu13=)	TEX26	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2242026	NM_152325.3(TEX26):c.69C>A (p.Asp23Glu)	TEX26 (D23E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2491513	NM_152325.3(TEX26):c.94A>G (p.Thr32Ala)	TEX26 (T32A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3176377	NM_152325.3(TEX26):c.149A>G (p.Gln50Arg)	TEX26 (Q50R)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2330483	NM_152325.3(TEX26):c.154G>A (p.Gly52Ser)	TEX26 (G52S)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GLikely benign
Select item 2558401	NM_152325.3(TEX26):c.209C>G (p.Thr70Arg)	TEX26 (T70R)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2235811	NM_152325.3(TEX26):c.226T>A (p.Tyr76Asn)	TEX26 (Y76N)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2297569	NM_152325.3(TEX26):c.281G>A (p.Gly94Glu)	TEX26 (G94E)	Single nucleotide variant (5 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2313175	NM_152325.3(TEX26):c.389C>T (p.Ala130Val)	TEX26 (A130V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2322292	NM_152325.3(TEX26):c.394A>G (p.Met132Val)	TEX26 (M1V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3176378	NM_152325.3(TEX26):c.403G>A (p.Val135Ile)	TEX26 (V135I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557810	NM_152325.3(TEX26):c.421A>T (p.Asn141Tyr)	TEX26 (N141Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3325568	NM_152325.3(TEX26):c.427T>C (p.Phe143Leu)	TEX26 (F12L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592090	NM_152325.3(TEX26):c.434C>T (p.Ser145Phe)	TEX26 (S14F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224746	NM_152325.3(TEX26):c.436C>T (p.Leu146Phe)	TEX26 (L146F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486574	NM_152325.3(TEX26):c.452T>C (p.Phe151Ser)	TEX26 (F151S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176379	NM_152325.3(TEX26):c.499T>A (p.Ser167Thr)	TEX26 (S36T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176380	NM_152325.3(TEX26):c.505G>C (p.Glu169Gln)	TEX26 (E38Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176381	NM_152325.3(TEX26):c.548G>A (p.Arg183Gln)	TEX26 (R183Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710812	NM_152325.3(TEX26):c.693G>T (p.Lys231Asn)	TEX26 (K100N +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2559125	NM_152325.3(TEX26):c.697C>G (p.Gln233Glu)	TEX26 (Q233E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176382	NM_152325.3(TEX26):c.707A>T (p.Tyr236Phe)	TEX26 (Y105F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176383	NM_152325.3(TEX26):c.721G>A (p.Asp241Asn)	TEX26 (D241N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308310	NM_152325.3(TEX26):c.755A>G (p.Asn252Ser)	TEX26 (N121S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3176384	NM_152325.3(TEX26):c.767C>A (p.Ser256Tyr)	TEX26 (S125Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26