"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TMPRSS3 - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1032152	NM_001256317.3(TMPRSS3):c.1360T>C (p.Ter454Arg)	TMPRSS3	Single nucleotide variant (stop lost)	Autosomal recessive nonsyndromic hearing loss 8 +2 more	GConflicting classifications of pathogenicity
Select item 2872574	NM_001256317.3(TMPRSS3):c.1350C>T (p.Asp450=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2706865	NM_001256317.3(TMPRSS3):c.1345-8A>C	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1559557	NM_001256317.3(TMPRSS3):c.1345-8A>G	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005009	NM_001256317.3(TMPRSS3):c.1345-19C>G	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2846545	NM_001256317.3(TMPRSS3):c.1345-19C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1908529	NM_001256317.3(TMPRSS3):c.1345-20G>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2863408	NM_001256317.3(TMPRSS3):c.1344+17C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1900512	NM_001256317.3(TMPRSS3):c.1344+12G>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960550	NM_001256317.3(TMPRSS3):c.1344+11C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 897376	NM_001256317.3(TMPRSS3):c.1344+9G>A	TMPRSS3	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 8 +1 more	GConflicting classifications of pathogenicity
Select item 897377	NM_001256317.3(TMPRSS3):c.1344+8C>T	TMPRSS3	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 8 +1 more	GConflicting classifications of pathogenicity
Select item 1909242	NM_001256317.3(TMPRSS3):c.1335_1339dup (p.Met447fs)	TMPRSS3 (M321fs +2 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 46104	NM_001256317.3(TMPRSS3):c.1340T>C (p.Met447Thr)	TMPRSS3 (M448T +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2631680	NM_001256317.3(TMPRSS3):c.1333G>A (p.Glu445Lys)	TMPRSS3 (E319K +2 more)	Single nucleotide variant (missense variant)	TMPRSS3-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 178547	NM_001256317.3(TMPRSS3):c.1332C>T (p.His444=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 2999992	NM_001256317.3(TMPRSS3):c.1308C>T (p.Val436=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 46103	NM_001256317.3(TMPRSS3):c.1306G>A (p.Val436Ile)	TMPRSS3 (V437I +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 8 +2 more	GConflicting classifications of pathogenicity
Select item 1961947	NM_001256317.3(TMPRSS3):c.1304G>A (p.Arg435His)	TMPRSS3 (R309H +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1509020	NM_001256317.3(TMPRSS3):c.1304G>C (p.Arg435Pro)	TMPRSS3 (R309P +2 more)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 666988	NM_001256317.3(TMPRSS3):c.1303C>T (p.Arg435Cys)	TMPRSS3 (R435C +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 8 +2 more	GConflicting classifications of pathogenicity
Select item 2839298	NM_001256317.3(TMPRSS3):c.1302C>T (p.Thr434=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 805672	NM_001256317.3(TMPRSS3):c.1293G>C (p.Gly431=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962610	NM_001256317.3(TMPRSS3):c.1290T>C (p.Pro430=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2736990	NM_001256317.3(TMPRSS3):c.1288C>T (p.Pro430Ser)	TMPRSS3 (P431S +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2700615	NM_001256317.3(TMPRSS3):c.1288C>A (p.Pro430Thr)	TMPRSS3 (P431T +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2818373	NM_001256317.3(TMPRSS3):c.1278G>A (p.Glu426=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 46102	NM_001256317.3(TMPRSS3):c.1273G>A (p.Ala425Thr)	TMPRSS3 (A426T +2 more)	Single nucleotide variant (missense variant)	Rare genetic deafness +3 more	GPathogenic/Likely pathogenic
Select item 46101	NM_001256317.3(TMPRSS3):c.1272C>T (p.Cys424=)	TMPRSS3	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 8 +2 more	GConflicting classifications of pathogenicity
Select item 595601	NM_001256317.3(TMPRSS3):c.1266C>T (p.Ile422=)	TMPRSS3	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 8 +1 more	GConflicting classifications of pathogenicity
Select item 2875788	NM_001256317.3(TMPRSS3):c.1263C>A (p.Gly421=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2877964	NM_001256317.3(TMPRSS3):c.1254C>T (p.Thr418=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2712249	NM_001256317.3(TMPRSS3):c.1251G>A (p.Ala417=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2116592	NM_001256317.3(TMPRSS3):c.1245G>A (p.Val415=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2699472	NM_001256317.3(TMPRSS3):c.1240T>C (p.Leu414=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2799787	NM_001256317.3(TMPRSS3):c.1239G>A (p.Lys413=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977711	NM_001256317.3(TMPRSS3):c.1231C>T (p.Leu411=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1064913	NM_001256317.3(TMPRSS3):c.1221del (p.Glu408fs)	TMPRSS3 (E282fs +2 more)	Deletion (frameshift variant)	Hearing impairment +1 more	GConflicting classifications of pathogenicity
Select item 996724	NM_001256317.3(TMPRSS3):c.1216T>C (p.Cys406Arg)	TMPRSS3 (C280R +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 8 +1 more	GPathogenic/Likely pathogenic
Select item 4945	NM_001256317.3(TMPRSS3):c.1208C>T (p.Pro403Leu)	TMPRSS3 (P404L +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 731856	NM_001256317.3(TMPRSS3):c.1206G>A (p.Gly402=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002449	NM_001256317.3(TMPRSS3):c.1203G>A (p.Gly401=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2755968	NM_001256317.3(TMPRSS3):c.1201G>T (p.Gly401Trp)	TMPRSS3 (G275W +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2138388	NM_001256317.3(TMPRSS3):c.1201G>A (p.Gly401Arg)	TMPRSS3 (G402R +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2985127	NM_001256317.3(TMPRSS3):c.1200C>T (p.Ser400=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2744477	NM_001256317.3(TMPRSS3):c.1194G>A (p.Gly398=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955316	NM_001256317.3(TMPRSS3):c.1192-4C>G	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2707327	NM_001256317.3(TMPRSS3):c.1192-4C>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 340058	NM_001256317.3(TMPRSS3):c.1192-8T>C	TMPRSS3	Single nucleotide variant (intron variant)	Hearing loss, autosomal recessive +1 more	GConflicting classifications of pathogenicity
Select item 2975915	NM_001256317.3(TMPRSS3):c.1192-11C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2003223	NM_001256317.3(TMPRSS3):c.1192-12C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2789493	NM_001256317.3(TMPRSS3):c.1192-16C>G	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2788495	NM_001256317.3(TMPRSS3):c.1192-16C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2858037	NM_001256317.3(TMPRSS3):c.1191+16G>C	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2787611	NM_001256317.3(TMPRSS3):c.1191+16G>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965417	NM_001256317.3(TMPRSS3):c.1191+15C>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1912977	NM_001256317.3(TMPRSS3):c.1191+15C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2858420	NM_001256317.3(TMPRSS3):c.1191+14G>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2780242	NM_001256317.3(TMPRSS3):c.1191+14G>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2836621	NM_001256317.3(TMPRSS3):c.1191+12C>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 180040	NM_001256317.3(TMPRSS3):c.1191+11G>A	TMPRSS3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 736897	NM_001256317.3(TMPRSS3):c.1191+10C>T	TMPRSS3	Single nucleotide variant (intron variant)	Autosomal recessive nonsyndromic hearing loss 8 +1 more	GConflicting classifications of pathogenicity
Select item 2876724	NM_001256317.3(TMPRSS3):c.1191+8G>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2791323	NM_001256317.3(TMPRSS3):c.1191+1G>A	TMPRSS3	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 1934530	NM_001256317.3(TMPRSS3):c.1180G>A (p.Asp394Asn)	TMPRSS3 (D394N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 46099	NM_001256317.3(TMPRSS3):c.1180G>C (p.Asp394His)	TMPRSS3 (D395H +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2743207	NM_001256317.3(TMPRSS3):c.1179G>C (p.Val393=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2964325	NM_001256317.3(TMPRSS3):c.1176C>T (p.Gly392=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2889630	NM_001256317.3(TMPRSS3):c.1170G>A (p.Thr390=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977534	NM_001256317.3(TMPRSS3):c.1167G>C (p.Leu389=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2873685	NM_001256317.3(TMPRSS3):c.1164C>T (p.Tyr388=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996492	NM_001256317.3(TMPRSS3):c.1158G>A (p.Ala386=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017257	NM_001256317.3(TMPRSS3):c.1157C>T (p.Ala386Val)	TMPRSS3 (A260V +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2772340	NM_001256317.3(TMPRSS3):c.1156G>C (p.Ala386Pro)	TMPRSS3 (A386P +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2736991	NM_001256317.3(TMPRSS3):c.1156G>A (p.Ala386Thr)	TMPRSS3 (A387T +2 more)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 517241	NM_001256317.3(TMPRSS3):c.1155C>T (p.Cys385=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2905368	NM_001256317.3(TMPRSS3):c.1152C>G (p.Leu384=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 165482	NM_001256317.3(TMPRSS3):c.1149G>T (p.Met383Ile)	TMPRSS3 (M384I +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 873474	NM_001256317.3(TMPRSS3):c.1148T>A (p.Met383Lys)	TMPRSS3 (M383K +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2776649	NM_001256317.3(TMPRSS3):c.1146C>T (p.Ser382=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1937587	NM_001256317.3(TMPRSS3):c.1146C>A (p.Ser382=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3000591	NM_001256317.3(TMPRSS3):c.1143C>T (p.Pro381=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2777549	NM_001256317.3(TMPRSS3):c.1140C>T (p.Ser380=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 46098	NM_001256317.3(TMPRSS3):c.1125C>T (p.Tyr375=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 46097	NM_001256317.3(TMPRSS3):c.1119C>T (p.Asp373=)	TMPRSS3	Single nucleotide variant (synonymous variant)	Autosomal recessive nonsyndromic hearing loss 8 +2 more	GConflicting classifications of pathogenicity
Select item 2764365	NM_001256317.3(TMPRSS3):c.1114A>C (p.Arg372=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2890303	NM_001256317.3(TMPRSS3):c.1113C>T (p.His371=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005389	NM_001256317.3(TMPRSS3):c.1107C>T (p.Cys369=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2910617	NM_001256317.3(TMPRSS3):c.1080C>T (p.Ala360=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 898535	NM_001256317.3(TMPRSS3):c.1077G>A (p.Ala359=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2742031	NM_001256317.3(TMPRSS3):c.1074C>T (p.His358=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1936355	NM_001256317.3(TMPRSS3):c.1066C>T (p.Leu356=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2794108	NM_001256317.3(TMPRSS3):c.1062T>C (p.Pro354=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880777	NM_001256317.3(TMPRSS3):c.1059C>G (p.Ser353=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 46095	NM_001256317.3(TMPRSS3):c.1053C>T (p.Asp351=)	TMPRSS3	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 2159764	NM_001256317.3(TMPRSS3):c.1049-4G>A	TMPRSS3	Single nucleotide variant (intron variant +1 more)	Autosomal recessive nonsyndromic hearing loss 8 +1 more	GLikely pathogenic
Select item 2848538	NM_001256317.3(TMPRSS3):c.1049-8T>G	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1922385	NM_001256317.3(TMPRSS3):c.1049-9T>C	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1588421	NM_001256317.3(TMPRSS3):c.1049-12A>T	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1199548	NM_001256317.3(TMPRSS3):c.1049-16A>G	TMPRSS3	Single nucleotide variant (intron variant)	not provided	GLikely benign

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