ClinVar for Gene (Select 7168) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3075681	NM_001018005.2(TPM1):c.430C>G (p.Gln144Glu)	TPM1 (Q108E +2 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1Y	GLikely pathogenic
Select item 3075404	NM_001018005.2(TPM1):c.804A>G (p.Lys268=)	TPM1	Single nucleotide variant (synonymous variant +3 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3075010	NM_001018005.2(TPM1):c.685T>C (p.Ser229Pro)	TPM1 (S193P +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3074931	NM_001018005.2(TPM1):c.318G>A (p.Leu106=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3074921	NM_001018005.2(TPM1):c.563+5G>A	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3074870	NM_001018005.2(TPM1):c.574G>T (p.Glu192Ter)	TPM1 (E156* +2 more)	Single nucleotide variant (nonsense +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3074858	NM_001018005.2(TPM1):c.835A>G (p.Asn279Asp)	TPM1 (N243D +2 more)	Single nucleotide variant (missense variant +3 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3074695	NM_001018005.2(TPM1):c.105G>A (p.Arg35=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3074587	NM_001018005.2(TPM1):c.849del (p.Ile284fs)	TPM1 (I248fs +5 more)	Deletion (frameshift variant +3 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3074531	NM_001018005.2(TPM1):c.354G>A (p.Lys118=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3074430	NM_001018005.2(TPM1):c.608A>T (p.Asn203Ile)	TPM1 (N167I +2 more)	Single nucleotide variant (missense variant +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3074310	NM_001018005.2(TPM1):c.36G>A (p.Lys12=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3074141	NM_001018005.2(TPM1):c.9C>T (p.Ala3=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3073997	NM_001018005.2(TPM1):c.682C>G (p.Leu228Val)	TPM1 (L192V +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3073702	NM_001018005.2(TPM1):c.581A>G (p.Glu194Gly)	TPM1 (E158G +2 more)	Single nucleotide variant (missense variant +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3073525	NM_001018005.2(TPM1):c.773-4A>T	TPM1	Single nucleotide variant (3 prime UTR variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3073286	NM_001018005.2(TPM1):c.274A>G (p.Ile92Val)	TPM1 (I134V +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3073123	NM_001018005.2(TPM1):c.773-10del	TPM1	Deletion (3 prime UTR variant +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3073114	NM_001018005.2(TPM1):c.436A>T (p.Ile146Phe)	TPM1 (I110F +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3073021	NM_001018005.2(TPM1):c.78G>A (p.Glu26=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3072548	NM_001018005.2(TPM1):c.51C>A (p.Asn17Lys)	TPM1 (N17K)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3072475	NM_001018005.2(TPM1):c.498C>T (p.Ala166=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3072399	NM_001018005.2(TPM1):c.640-10C>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3072395	NM_001018005.2(TPM1):c.628C>T (p.Gln210Ter)	TPM1 (Q174* +2 more)	Single nucleotide variant (nonsense +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3072370	NM_001018005.2(TPM1):c.812G>A (p.Ser271Asn)	TPM1 (S235N +2 more)	Single nucleotide variant (missense variant +3 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3072014	NM_001018005.2(TPM1):c.270A>G (p.Arg90=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3071679	NM_001018005.2(TPM1):c.528G>A (p.Leu176=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3071415	NM_001018005.2(TPM1):c.603G>A (p.Thr201=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3071288	NM_001018005.2(TPM1):c.114+1G>A	TPM1	Single nucleotide variant (splice donor variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3070988	NM_001018005.2(TPM1):c.264G>T (p.Leu88=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3070877	NM_001018005.2(TPM1):c.414A>G (p.Glu138=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3070275	NM_001018005.2(TPM1):c.432G>A (p.Gln144=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3070271	NM_001018005.2(TPM1):c.513C>A (p.Ile171=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3069791	NM_001018005.2(TPM1):c.237C>T (p.Thr79=)	TPM1	Single nucleotide variant (synonymous variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3069588	NM_001018005.2(TPM1):c.241-13A>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3069359	NM_001018005.2(TPM1):c.493-9C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3069284	NM_001018005.2(TPM1):c.819G>T (p.Glu273Asp)	TPM1 (E237D +2 more)	Single nucleotide variant (missense variant +3 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3069216	NM_001018005.2(TPM1):c.397C>T (p.Arg133Ter)	TPM1 (R133* +2 more)	Single nucleotide variant (nonsense +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 3064898	NM_001018005.2(TPM1):c.115-276G>A	TPM1 (E54K)	Single nucleotide variant (missense variant +2 more)	Dilated cardiomyopathy 1Y	GUncertain significance
Select item 3061182	NM_001018005.2(TPM1):c.720G>C (p.Glu240Asp)	TPM1 (E204D +2 more)	Single nucleotide variant (missense variant +1 more)	TPM1-related condition	GUncertain significance
Select item 3025133	NM_001018005.2(TPM1):c.772+98C>T	TPM1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3017442	NM_001018005.2(TPM1):c.703-16A>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3000506	NM_001018005.2(TPM1):c.114+15G>C	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 3000074	NM_001018005.2(TPM1):c.703-8C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2998539	NM_001018005.2(TPM1):c.492+19A>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2974720	NM_001018005.2(TPM1):c.114+19C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2971067	NM_001018005.2(TPM1):c.326C>T (p.Ala109Val)	TPM1 (A109V +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2964267	NM_001018005.2(TPM1):c.772+14T>C	TPM1	Single nucleotide variant (synonymous variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2963949	NM_001018005.2(TPM1):c.492+19A>C	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2957553	NM_001018005.2(TPM1):c.114+20T>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2957175	NM_001018005.2(TPM1):c.563+15C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2918248	NM_001018005.2(TPM1):c.702+6A>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2917423	NM_001018005.2(TPM1):c.183T>C (p.Ser61=)	TPM1	Single nucleotide variant (synonymous variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2912642	NM_001018005.2(TPM1):c.115-19C>T	TPM1	Single nucleotide variant (non-coding transcript variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2912069	NM_001018005.2(TPM1):c.492+11G>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2906838	NM_001018005.2(TPM1):c.687C>G (p.Ser229=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2905506	NM_001018005.2(TPM1):c.297G>A (p.Leu99=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2904897	NM_001018005.2(TPM1):c.523G>T (p.Asp175Tyr)	TPM1 (D175Y +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2897519	NM_001018005.2(TPM1):c.564-14A>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2892831	NM_001018005.2(TPM1):c.832C>T (p.Leu278Phe)	TPM1 (L278F +1 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2892108	NM_001018005.2(TPM1):c.563+17C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2882165	NM_001018005.2(TPM1):c.772+15A>G	TPM1 (S263G +1 more)	Single nucleotide variant (missense variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2876852	NM_001018005.2(TPM1):c.590T>C (p.Leu197Ser)	TPM1 (L239S +2 more)	Single nucleotide variant (non-coding transcript variant +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2870254	NM_001018005.2(TPM1):c.619C>T (p.Leu207=)	TPM1	Single nucleotide variant (synonymous variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2863296	NM_001018005.2(TPM1):c.813C>G (p.Ser271Arg)	TPM1 (S235R +2 more)	Single nucleotide variant (missense variant +3 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2857343	NM_001018005.2(TPM1):c.851+7del	TPM1	Deletion (3 prime UTR variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2856994	NM_001018005.2(TPM1):c.374+16C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2853533	NM_001018005.2(TPM1):c.24_25delinsAA (p.Met8_Gln9delinsIleLys)	TPM1	Indel (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2850868	NM_001018005.2(TPM1):c.52G>A (p.Ala18Thr)	TPM1 (A18T)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GLikely pathogenic
Select item 2849500	NM_001018005.2(TPM1):c.22A>G (p.Met8Val)	TPM1 (M8V)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2842476	NM_001018005.2(TPM1):c.810C>G (p.Ile270Met)	TPM1 (I270M +2 more)	Single nucleotide variant (missense variant +3 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2841824	NM_001018005.2(TPM1):c.115-7C>G	TPM1	Single nucleotide variant (non-coding transcript variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2839441	NM_001018005.2(TPM1):c.564-11dup	TPM1	Duplication (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2839440	NM_001018005.2(TPM1):c.760G>A (p.Asp254Asn)	TPM1 (D218N +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2839372	NM_001018005.2(TPM1):c.43A>G (p.Lys15Glu)	TPM1 (K15E)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2834088	NM_001018005.2(TPM1):c.161A>C (p.Glu54Ala)	TPM1 (E96A +1 more)	Single nucleotide variant (missense variant +2 more)	Hypertrophic cardiomyopathy	GLikely pathogenic
Select item 2833135	NM_001018005.2(TPM1):c.433G>A (p.Glu145Lys)	TPM1 (E187K +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GLikely pathogenic
Select item 2826576	NM_001018005.2(TPM1):c.114+12C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2822493	NM_001018005.2(TPM1):c.831T>C (p.Ala277=)	TPM1	Single nucleotide variant (synonymous variant +3 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2821495	NM_001018005.2(TPM1):c.214G>T (p.Glu72Ter)	TPM1 (E72* +1 more)	Single nucleotide variant (nonsense +2 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2821257	NM_001018005.2(TPM1):c.240+16C>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2818935	NM_001018005.2(TPM1):c.375-4del	TPM1	Deletion (intron variant)	Hypertrophic cardiomyopathy	GBenign
Select item 2814387	NM_001018005.2(TPM1):c.639+20T>C	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2810519	NM_001018005.2(TPM1):c.505C>G (p.Leu169Val)	TPM1 (L133V +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2807361	NM_001018005.2(TPM1):c.493-9del	TPM1	Deletion (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2805431	NM_001018005.2(TPM1):c.772+16G>A	TPM1 (S227N +1 more)	Single nucleotide variant (missense variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2794362	NM_001018005.2(TPM1):c.563+3A>G	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2789832	NM_001018005.2(TPM1):c.564-15G>T	TPM1	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2785893	NM_001018005.2(TPM1):c.772+8C>T	TPM1	Single nucleotide variant (synonymous variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2785615	NM_001018005.2(TPM1):c.162A>G (p.Glu54=)	TPM1	Single nucleotide variant (synonymous variant +2 more)	Hypertrophic cardiomyopathy	GLikely benign
Select item 2780214	NM_001018005.2(TPM1):c.331C>G (p.Gln111Glu)	TPM1 (Q111E +2 more)	Single nucleotide variant (missense variant +1 more)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 2774665	NM_001018005.2(TPM1):c.852-12A>T	TPM1	Single nucleotide variant (3 prime UTR variant +2 more)	Cardiomyopathy	GLikely benign
Select item 2774664	NM_001018005.2(TPM1):c.207G>T (p.Glu69Asp)	TPM1 (E111D +1 more)	Single nucleotide variant (intron variant +2 more)	Cardiomyopathy	GUncertain significance
Select item 2774663	NM_001018005.2(TPM1):c.103A>C (p.Arg35=)	TPM1	Single nucleotide variant (synonymous variant +1 more)	Cardiomyopathy	GLikely benign
Select item 2774662	NM_001018005.2(TPM1):c.100G>A (p.Asp34Asn)	TPM1 (D34N)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy	GUncertain significance
Select item 2774661	NM_001018005.2(TPM1):c.95C>T (p.Ala32Val)	TPM1 (A32V)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy +1 more	GUncertain significance
Select item 2774660	NM_001018005.2(TPM1):c.79G>A (p.Ala27Thr)	TPM1 (A27T)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy	GUncertain significance
Select item 2774659	NM_001018005.2(TPM1):c.-7C>T	TPM1	Single nucleotide variant (5 prime UTR variant +1 more)	Cardiomyopathy	GUncertain significance
Select item 2774658	NM_001018005.2(TPM1):c.-10C>T	TPM1	Single nucleotide variant (5 prime UTR variant +1 more)	Cardiomyopathy	GUncertain significance
Select item 2774657	NM_001018005.2(TPM1):c.-12G>A	TPM1	Single nucleotide variant (5 prime UTR variant +1 more)	Cardiomyopathy	GUncertain significance

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