NM_003977.4(AIP):c.121C>G (p.Leu41Val) AND not provided

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 24, 2023
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:: RCV003696279.1

Allele description

NM_003977.4(AIP):c.121C>G (p.Leu41Val)

Genes:

LOC130006206:ATAC-STARR-seq lymphoblastoid active region 5107 [Gene]
AIP:aryl hydrocarbon receptor interacting protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.2

Genomic location:

Preferred name:

NM_003977.4(AIP):c.121C>G (p.Leu41Val)

HGVS:

NC_000011.10:g.67487027C>G
NG_008969.1:g.8994C>G
NG_185651.1:g.253C>G
NM_001302959.2:c.-57C>G
NM_001302960.2:c.121C>G
NM_003977.4:c.121C>GMANE SELECT
NP_001289889.1:p.Leu41Val
NP_003968.2:p.Leu41Val
NP_003968.3:p.Leu41Val
LRG_460t1:c.121C>G
LRG_460:g.8994C>G
LRG_460p1:p.Leu41Val
NC_000011.9:g.67254498C>G
NM_003977.2:c.121C>G

Protein change:

L41V

Molecular consequence:

NM_001302959.2:c.-57C>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001302960.2:c.121C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003977.4:c.121C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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Restoration genetics sample of Arabis nemorensis x Arabis sagittata natural hybr...
Restoration genetics sample of Arabis nemorensis x Arabis sagittata natural hybrid

biosample
CBSW4031.g1 NICHD_XGC_tropTail_m Xenopus tropicalis cDNA clone IMAGE:8906137 3',...
CBSW4031.g1 NICHD_XGC_tropTail_m Xenopus tropicalis cDNA clone IMAGE:8906137 3', mRNA sequence
gi|133760016|gnl|dbEST|45193211|gb| 271.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004455371	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Nov 24, 2023)	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

SCV004455371

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Nov 24, 2023)

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 Invitae, SCV004455371.1

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

Description

This sequence change replaces leucine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 41 of the AIP protein (p.Leu41Val). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with AIP-related conditions. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt AIP protein function with a negative predictive value of 80%. 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.

#	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: Feb 28, 2024

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