"GeneDx"[submitter] AND "MYL4"[gene] - ClinVar

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

Search results

Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1284100	NM_002476.2(MYL4):c.135+197G>A	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221612	NM_002476.2(MYL4):c.136-277T>G	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1223029	NM_002476.2(MYL4):c.136-137A>G	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316901	NM_002476.2(MYL4):c.136-106G>A	MYL4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1178801	NM_002476.2(MYL4):c.136-56del	MYL4	Deletion (intron variant)	not provided	GBenign
Select item 476198	NM_002476.2(MYL4):c.150C>T (p.Ala50=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18 +1 more	GBenign/Likely benign
Select item 1237126	NM_002476.2(MYL4):c.163+46GGA[8]	MYL4	Microsatellite (intron variant)	not provided	GBenign
Select item 1242408	NM_002476.2(MYL4):c.164-266C>T	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221863	NM_002476.2(MYL4):c.164-157G>T	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251632	NM_002476.2(MYL4):c.164-145C>G	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178474	NM_002476.2(MYL4):c.164-18T>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18 +1 more	GBenign
Select item 476199	NM_002476.2(MYL4):c.167T>C (p.Phe56Ser)	MYL4 (F56S)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18 +1 more	GConflicting classifications of pathogenicity
Select item 705545	NM_002476.2(MYL4):c.201G>A (p.Pro67=)	MYL4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1268761	NM_002476.2(MYL4):c.313+174G>A	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270156	NM_002476.2(MYL4):c.314-119T>A	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 476202	NM_002476.2(MYL4):c.314-4G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18 +1 more	GBenign
Select item 1261120	NM_002476.2(MYL4):c.487+73C>T	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231583	NM_002476.2(MYL4):c.487+141T>C	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290599	NM_002476.2(MYL4):c.488-154G>C	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1316974	NM_002476.2(MYL4):c.488-75G>A	MYL4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 476206	NM_002476.2(MYL4):c.488-4G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18 +1 more	GBenign/Likely benign
Select item 476210	NM_002476.2(MYL4):c.556A>T (p.Asn186Tyr)	MYL4 (N186Y)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18 +1 more	GBenign
Select item 1257549	NM_002476.2(MYL4):c.566-162C>T	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265045	NM_002476.2(MYL4):c.566-40C>T	MYL4	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 24