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NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile) AND multiple conditions

Germline classification:
Likely benign (1 submission)
Last evaluated:
Sep 27, 2021
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:
RCV002502142.8

Allele description [Variation Report for NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)]

NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)

Gene:
GLI3:GLI family zinc finger 3 [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
7p14.1
Genomic location:
Preferred name:
NM_000168.6(GLI3):c.3083_3084delinsTT (p.Ser1028Ile)
HGVS:
  • NC_000007.14:g.41965989_41965990delinsAA
  • NG_008434.1:g.276031_276032delinsTT
  • NM_000168.6:c.3083_3084delinsTTMANE SELECT
  • NP_000159.3:p.Ser1028Ile
  • NC_000007.13:g.42005587_42005588delinsAA
  • NM_000168.5:c.3083_3084delGCinsTT
  • NM_000168.5:c.3083_3084delinsTT
Protein change:
S1028I
Links:
dbSNP: rs886043721
NCBI 1000 Genomes Browser:
rs886043721
Molecular consequence:
  • NM_000168.6:c.3083_3084delinsTT - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Greig cephalopolysyndactyly syndrome (GCPS)
Synonyms:
Greig syndrome; Polysyndactyly with peculiar skull shape
Identifiers:
MONDO: MONDO:0008287; MedGen: C0265306; Orphanet: 380; OMIM: 175700
Name:
Pallister-Hall syndrome (PHS)
Synonyms:
Hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly
Identifiers:
MONDO: MONDO:0007804; MedGen: C0265220; Orphanet: 672; OMIM: 146510
Name:
Polysyndactyly 4
Synonyms:
Polysyndactyly uncomplicated; Preaxial polydactyly 4
Identifiers:
MONDO: MONDO:0008272; MedGen: C1868111; Orphanet: 93338; OMIM: 174700
Name:
Polydactyly, postaxial, type A1
Identifiers:
MONDO: MONDO:0008266; MedGen: C4282400; OMIM: 174200

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002807308Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benign
(Sep 27, 2021) 		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

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002807308.1

#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 10, 2024