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NM_015272.5(RPGRIP1L):c.2968CCT[2] (p.Pro992del) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 24, 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:
RCV002504405.1

Allele description [Variation Report for NM_015272.5(RPGRIP1L):c.2968CCT[2] (p.Pro992del)]

NM_015272.5(RPGRIP1L):c.2968CCT[2] (p.Pro992del)

Gene:
RPGRIP1L:RPGRIP1 like [Gene - OMIM - HGNC]
Variant type:
Microsatellite
Cytogenetic location:
16q12.2
Genomic location:
Preferred name:
NM_015272.5(RPGRIP1L):c.2968CCT[2] (p.Pro992del)
HGVS:
  • NC_000016.10:g.53638396GAG[2]
  • NG_008991.2:g.70458CCT[2]
  • NM_001127897.4:c.2959-548CCT[2]
  • NM_001308334.3:c.2968CCT[2]
  • NM_001330538.2:c.2959-548CCT[2]
  • NM_015272.5:c.2968CCT[2]MANE SELECT
  • NM_015272.5:c.2974_2976del
  • NP_001295263.1:p.Pro992del
  • NP_056087.2:p.Pro992del
  • LRG_696t1:c.2959-548CCT[2]
  • LRG_696t2:c.2968CCT[2]
  • LRG_696:g.70458CCT[2]
  • LRG_696p2:p.Pro992del
  • NC_000016.9:g.53672306_53672308del
  • NC_000016.9:g.53672308GAG[2]
  • NM_015272.4:c.2974_2976delCCT
  • NM_015272.5:c.2974_2976delMANE SELECT
  • NM_015272.5:c.2974_2976delCCTMANE SELECT
Protein change:
P992del
Links:
dbSNP: rs752076060
NCBI 1000 Genomes Browser:
rs752076060
Molecular consequence:
  • NM_001308334.3:c.2968CCT[2] - inframe_deletion - [Sequence Ontology: SO:0001822]
  • NM_015272.5:c.2968CCT[2] - inframe_deletion - [Sequence Ontology: SO:0001822]
  • NM_001127897.4:c.2959-548CCT[2] - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001330538.2:c.2959-548CCT[2] - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Joubert syndrome 7 (JBTS7)
Identifiers:
MONDO: MONDO:0012694; MedGen: C1969053; Orphanet: 220497; OMIM: 611560
Name:
Meckel syndrome, type 5 (MKS5)
Identifiers:
MONDO: MONDO:0012695; MedGen: C1969052; Orphanet: 564; OMIM: 611561
Name:
COACH syndrome 3
Identifiers:
MONDO: MONDO:0030862; MedGen: C5436841; OMIM: 619113

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002815906Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Mar 24, 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

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002815906.1

#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 24, 2024