NM_002528.7(NTHL1):c.305T>G (p.Val102Gly) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 12, 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:: RCV001878999.5

Allele description [Variation Report for NM_002528.7(NTHL1):c.305T>G (p.Val102Gly)]

NM_002528.7(NTHL1):c.305T>G (p.Val102Gly)

Gene:

NTHL1:nth like DNA glycosylase 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16p13.3

Genomic location:

Preferred name:

NM_002528.7(NTHL1):c.305T>G (p.Val102Gly)

HGVS:

NC_000016.10:g.2046177A>C
NG_005895.1:g.1872A>C
NG_008412.1:g.6690T>G
NM_001318193.2:c.305T>G
NM_001318194.2:c.24+103T>G
NM_002528.7:c.305T>GMANE SELECT
NP_001305122.2:p.Val102Gly
NP_002519.2:p.Val102Gly
LRG_1366t1:c.305T>G
LRG_1366:g.6690T>G
LRG_1366p1:p.Val102Gly
LRG_487:g.1872A>C
NC_000016.9:g.2096178A>C

Protein change:

V102G

Links:

dbSNP: rs2150945430

NCBI 1000 Genomes Browser:

rs2150945430

Molecular consequence:

NM_001318194.2:c.24+103T>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001318193.2:c.305T>G - missense variant - [Sequence Ontology: SO:0001583]
NM_002528.7:c.305T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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ABC transporter ATP-binding protein [Thomasclavelia spiroformis]
ABC transporter ATP-binding protein [Thomasclavelia spiroformis]
gi|490746648|ref|WP_004608956.1|

Protein
PREDICTED: Homo sapiens multiple inositol-polyphosphate phosphatase 1 (MINPP1), ...
PREDICTED: Homo sapiens multiple inositol-polyphosphate phosphatase 1 (MINPP1), transcript variant X1, mRNA
gi|2462522002|ref|XM_054367221.1|

Nucleotide
Pathogen: clinical or host-associated sample from Streptococcus agalactiae
Pathogen: clinical or host-associated sample from Streptococcus agalactiae

biosample
PREDICTED: Piliocolobus tephrosceles ISG15 ubiquitin like modifier (ISG15), mRNA
PREDICTED: Piliocolobus tephrosceles ISG15 ubiquitin like modifier (ISG15), mRNA
gi|1788669918|ref|XM_023192830.2|

Nucleotide
Streptococcus agalactiae strain SH2515, whole genome shotgun sequencing project
Streptococcus agalactiae strain SH2515, whole genome shotgun sequencing project
gi|825919641|gb|LDAK00000000.1|LDAK 000

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002143869	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Feb 12, 2021)	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

SCV002143869

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Feb 12, 2021)

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, SCV002143869.2

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

Description

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 missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Not Available"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Not Available"). This variant has not been reported in the literature in individuals with NTHL1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces valine with glycine at codon 110 of the NTHL1 protein (p.Val110Gly). The valine residue is highly conserved and there is a moderate physicochemical difference between valine and glycine.

#	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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