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Links from Gene

Items: 1 to 100 of 1153

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBCEL-TECTA, TECTA
(I1102M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(G1104V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA, TBCEL-TECTA
(C260F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TBCEL-TECTA, TECTA
(G390R +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 21
GUncertain significance
TBCEL-TECTA, TECTA
Single nucleotide variant
(intron variant)
Autosomal dominant nonsyndromic hearing loss 12
+1 more
GUncertain significance
TBCEL-TECTA, TECTA
(S2120T +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
+1 more
GUncertain significance
TBCEL-TECTA, TECTA
(D505H +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
+1 more
GUncertain significance
TBCEL-TECTA, TECTA
(T1976P +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(V415I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(I1846S +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 21
GUncertain significance
TBCEL-TECTA, TECTA
(M1811del +1 more)
Deletion
Nonsyndromic genetic hearing loss
GUncertain significance
TECTA, TBCEL-TECTA
(K1726N +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
GUncertain significance
TBCEL-TECTA, TECTA
(D361E +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
GUncertain significance
TBCEL-TECTA, TECTA
(N455S +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
GUncertain significance
TBCEL-TECTA, TECTA
(N1538S +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
GUncertain significance
TBCEL-TECTA, TECTA
(V1182I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(T280A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(C1622R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(C1427Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
Single nucleotide variant
(splice donor variant)
Autosomal recessive nonsyndromic hearing loss 21
GLikely pathogenic
TBCEL-TECTA, TECTA
(C1408* +1 more)
Single nucleotide variant
(nonsense)
Autosomal recessive nonsyndromic hearing loss 21
GPathogenic
TBCEL-TECTA, TECTA
Single nucleotide variant
(synonymous variant)
not specified
GUncertain significance
TECTA, TBCEL-TECTA
(G1478F +1 more)
Indel
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(D511E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(P1133R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(C1704S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(E1715G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(G1492R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(I1868F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(E1148K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
(D1210G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(E1901K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(V1963F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(C1464S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(V2026D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA
(P1078A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA
(S2127L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA
(D1558Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA
(S158R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA
(T1074I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TECTA
(C1122F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
(R1278W +1 more)
Single nucleotide variant
(missense variant)
TECTA-related disorder
GUncertain significance
TBCEL-TECTA, TECTA
Single nucleotide variant
(intron variant)
TECTA-related disorder
GLikely benign
TBCEL-TECTA, TECTA
(T261A +1 more)
Single nucleotide variant
(missense variant)
TECTA-related disorder
GUncertain significance
TBCEL-TECTA, TECTA
(D102N +1 more)
Single nucleotide variant
(missense variant)
TECTA-related disorder
GUncertain significance
TBCEL-TECTA, TECTA
(S158fs +1 more)
Duplication
(frameshift variant)
TECTA-related disorder
GLikely pathogenic
TBCEL-TECTA, TECTA
(W100R +1 more)
Single nucleotide variant
(missense variant)
TECTA-related disorder
GUncertain significance
TBCEL-TECTA, TECTA
(G2078R +1 more)
Single nucleotide variant
(missense variant)
TECTA-related disorder
GUncertain significance
TBCEL-TECTA, TECTA
(E1998G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(E291D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(Q442fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
TBCEL-TECTA, TECTA
(A1982D +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely pathogenic
TBCEL-TECTA, TECTA
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBCEL-TECTA, TECTA
(Y1900C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
TBCEL-TECTA, TECTA
Single nucleotide variant
(intron variant)
Hearing impairment
GUncertain significance
TBCEL-TECTA, TECTA
(V1384fs +1 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
TBCEL-TECTA, TECTA
(A16T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(D553E +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(T1482S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(K1609M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(G1738W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(V1618A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(P646R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(T192M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
(E1195Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
(G1291E +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(T1446A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(F2027V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(R1150Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(H1944R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(L409F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(T546I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(E2326K +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBCEL-TECTA, TECTA
(T165I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(C1619Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBCEL-TECTA, TECTA
(E1015K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
(A1191S +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 21
GLikely pathogenic
TBCEL-TECTA, TECTA
(G434V +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
GLikely pathogenic
TBCEL-TECTA, TECTA
(F406C +1 more)
Single nucleotide variant
(missense variant)
Autosomal dominant nonsyndromic hearing loss 12
GUncertain significance
TBCEL-TECTA, TECTA
(D1769Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBCEL-TECTA, TECTA
(R1243C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC126861365, TBCEL-TECTA
+1 more
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
TBCEL-TECTA, TECTA
Single nucleotide variant
(intron variant)
not specified
GLikely benign
TBCEL-TECTA, TECTA
(R268Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(T536I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(E2403K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(V2391L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(E2383D +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(N2195D +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(E1776K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(D173N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(L1472M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(P1706L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(N1306I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(N1245S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(S1551N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TBCEL-TECTA, TECTA
(V1218I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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