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NM_002476.2(MYL4):c.353C>G (p.Pro118Arg)

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Interpretation:
Uncertain significance​

Review status:
criteria provided, single submitter
Submissions:
1 (Most recent: Jan 7, 2021)
Last evaluated:
Oct 16, 2020
Accession:
VCV001021850.1
Variation ID:
1021850
Description:
single nucleotide variant
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NM_002476.2(MYL4):c.353C>G (p.Pro118Arg)

Allele ID
1012832
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
17q21.32
Genomic location
17: 47221721 (GRCh38) GRCh38 UCSC
17: 45299087 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NC_000017.10:g.45299087C>G
NC_000017.11:g.47221721C>G
NG_052847.1:g.17705C>G
... more HGVS
Protein change
P118R
Other names
-
Canonical SPDI
NC_000017.11:47221720:C:G
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
-
Links
Varsome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Uncertain significance 1 criteria provided, single submitter Oct 16, 2020 RCV001321680.1
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
MYL4 - - GRCh38
GRCh37
84 93

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
Uncertain significance
(Oct 16, 2020)
criteria provided, single submitter
Method: clinical testing
Atrial fibrillation, familial, 18
Allele origin: germline
Invitae
Accession: SCV001512521.1
Submitted: (Jan 07, 2021)
Evidence details
Comment:
This sequence change replaces proline with arginine at codon 118 of the MYL4 protein (p.Pro118Arg). The proline residue is highly conserved and there is a … (more)

Functional evidence

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There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for this variant

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There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar.

Record last updated Oct 08, 2021