NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr) AND MYH7-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004541080.2
Allele description [Variation Report for NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)]
NM_000257.4(MYH7):c.4909G>A (p.Ala1637Thr)
Condition(s)
- Name:
- MYH7-related disorder
- Synonyms:
- MYH7-related condition; MYH7-Related Disorders; MYH7-related disease
- Identifiers:
-
zinc finger protein 747 isoform 3 [Homo sapiens]
zinc finger protein 747 isoform 3 [Homo sapiens]gi|13027594|ref|NP_076420.1|Protein
-
Homo sapiens FXYD domain containing ion transport regulator 3 (FXYD3), transcrip...
Homo sapiens FXYD domain containing ion transport regulator 3 (FXYD3), transcript variant 1, mRNAgi|1677539286|ref|NM_005971.4|Nucleotide
-
Homo sapiens rearranged immunoglobulin heavy chain variable region (ML6-VH4) mRN...
Homo sapiens rearranged immunoglobulin heavy chain variable region (ML6-VH4) mRNA, partial cdsgi|2232222|gb|AF004936.1|Nucleotide
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Last Updated: Oct 13, 2024