NM_014336.5(AIPL1):c.1095G>T (p.Gly365=) AND Leber congenital amaurosis 4

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 25, 2020
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:: RCV001322016.7

Allele description [Variation Report for NM_014336.5(AIPL1):c.1095G>T (p.Gly365=)]

NM_014336.5(AIPL1):c.1095G>T (p.Gly365=)

Gene:

AIPL1:aryl hydrocarbon receptor interacting protein like 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.2

Genomic location:

Preferred name:

NM_014336.5(AIPL1):c.1095G>T (p.Gly365=)

HGVS:

NC_000017.11:g.6425520C>A
NG_008474.1:g.14680G>T
NM_001033054.3:c.906G>T
NM_001033055.3:c.915G>T
NM_001285399.3:c.1059G>T
NM_001285400.3:c.1029G>T
NM_001285401.3:c.1023G>T
NM_001285402.2:c.978G>T
NM_001285403.4:c.*1066G>T
NM_014336.5:c.1095G>TMANE SELECT
NP_001028226.1:p.Gly302=
NP_001028227.1:p.Gly305=
NP_001272328.1:p.Gly353=
NP_001272329.1:p.Gly343=
NP_001272330.1:p.Gly341=
NP_001272331.1:p.Gly326=
NP_055151.3:p.Gly365=
NC_000017.10:g.6328840C>A

Links:

dbSNP: rs1911829075

NCBI 1000 Genomes Browser:

rs1911829075

Molecular consequence:

NM_001285403.4:c.*1066G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001033054.3:c.906G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001033055.3:c.915G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001285399.3:c.1059G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001285400.3:c.1029G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001285401.3:c.1023G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001285402.2:c.978G>T - synonymous variant - [Sequence Ontology: SO:0001819]
NM_014336.5:c.1095G>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Leber congenital amaurosis 4 (LCA4)
Synonyms:: Amaurosis congenita of Leber, type 4
Identifiers:: MONDO: MONDO:0011458; MedGen: C1858386; OMIM: 604393

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001512868	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Dec 25, 2020)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001512868

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Dec 25, 2020)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001512868.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

This variant is not present in population databases (ExAC no frequency). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has not been reported in the literature in individuals with AIPL1-related conditions. This sequence change affects codon 365 of the AIPL1 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the AIPL1 protein.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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