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NM_006662.3(SRCAP):c.62C>T (p.Ser21Leu) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 13, 2022
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV002478591.8

Allele description [Variation Report for NM_006662.3(SRCAP):c.62C>T (p.Ser21Leu)]

NM_006662.3(SRCAP):c.62C>T (p.Ser21Leu)

Gene:
SRCAP:Snf2 related CREBBP activator protein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p11.2
Genomic location:
Preferred name:
NM_006662.3(SRCAP):c.62C>T (p.Ser21Leu)
HGVS:
  • NC_000016.10:g.30704071C>T
  • NG_032135.1:g.9931C>T
  • NM_006662.3:c.62C>TMANE SELECT
  • NP_006653.2:p.Ser21Leu
  • NC_000016.9:g.30715392C>T
  • NM_006662.2:c.62C>T
Protein change:
S21L
Links:
dbSNP: rs183497403
NCBI 1000 Genomes Browser:
rs183497403
Molecular consequence:
  • NM_006662.3:c.62C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Floating-Harbor syndrome (FLHS)
Synonyms:
Short stature with delayed bone age, expressive language delay, a triangular face with a prominent nose and deep-set eyes; Pelletier-Leisti syndrome
Identifiers:
MONDO: MONDO:0007621; MedGen: C0729582; Orphanet: 2044; OMIM: 136140
Name:
Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities
Identifiers:
MONDO: MONDO:0859202; MedGen: C5562012; OMIM: 619595

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000896542Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(May 13, 2022) 		unknownclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753
PMC

Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL.

Genetics in medicine : official journal of the American College of Medical Genetics. 2015 Mar 5; 17(5): 405-424

PMC [article]
PMCID:
PMC4544753
PMID:
25741868
DOI:
10.1038/gim.2015.30

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV000896542.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 24, 2024