NM_001190737.2(NFIB):c.1292C>G (p.Thr431Ser) AND Inborn genetic diseases

Germline classification:: Likely benign (1 submission)
Last evaluated:: Dec 14, 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:: RCV004369889.1

Allele description [Variation Report for NM_001190737.2(NFIB):c.1292C>G (p.Thr431Ser)]

NM_001190737.2(NFIB):c.1292C>G (p.Thr431Ser)

Gene:

NFIB:nuclear factor I B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9p23

Genomic location:

Preferred name:

NM_001190737.2(NFIB):c.1292C>G (p.Thr431Ser)

HGVS:

NC_000009.12:g.14116300G>C
NM_001190737.2:c.1292C>GMANE SELECT
NM_001190738.2:c.1323+4140C>G
NM_001282787.2:c.536C>G
NM_001369458.1:c.1358C>G
NM_001369459.1:c.1358C>G
NM_001369460.1:c.1280C>G
NM_001369461.1:c.1292C>G
NM_001369462.1:c.1311+4140C>G
NM_001369463.1:c.1280C>G
NM_001369464.1:c.1245+4140C>G
NM_001369465.1:c.1265C>G
NM_001369466.1:c.1233+4140C>G
NM_001369467.1:c.1218+4140C>G
NM_001369468.1:c.1311+4140C>G
NM_001369469.1:c.1101+4140C>G
NM_001369470.1:c.1055C>G
NM_001369471.1:c.1242+4140C>G
NM_001369472.1:c.1233+4140C>G
NM_001369473.1:c.1230+4140C>G
NM_001369474.1:c.1227+4140C>G
NM_001369475.1:c.1020+4140C>G
NM_001369476.1:c.1218+4140C>G
NM_001369477.1:c.1188+4140C>G
NM_001369478.1:c.1008+4140C>G
NM_001369479.1:c.708+4140C>G
NM_001369480.1:c.708+4140C>G
NM_005596.3:c.1245+4140C>G
NP_001177666.1:p.Thr431Ser
NP_001269716.1:p.Thr179Ser
NP_001356387.1:p.Thr453Ser
NP_001356388.1:p.Thr453Ser
NP_001356389.1:p.Thr427Ser
NP_001356390.1:p.Thr431Ser
NP_001356392.1:p.Thr427Ser
NP_001356394.1:p.Thr422Ser
NP_001356399.1:p.Thr352Ser
NC_000009.11:g.14116299G>C
NM_001190737.1:c.1292C>G

Protein change:

T179S

Molecular consequence:

NM_001190738.2:c.1323+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369462.1:c.1311+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369464.1:c.1245+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369466.1:c.1233+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369467.1:c.1218+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369468.1:c.1311+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369469.1:c.1101+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369471.1:c.1242+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369472.1:c.1233+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369473.1:c.1230+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369474.1:c.1227+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369475.1:c.1020+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369476.1:c.1218+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369477.1:c.1188+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369478.1:c.1008+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369479.1:c.708+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001369480.1:c.708+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_005596.3:c.1245+4140C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001190737.2:c.1292C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001282787.2:c.536C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369458.1:c.1358C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369459.1:c.1358C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369460.1:c.1280C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369461.1:c.1292C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369463.1:c.1280C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369465.1:c.1265C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369470.1:c.1055C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004988674	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Dec 14, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004988674

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Dec 14, 2023)

germline

clinical testing

Citation Link

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

Details of each submission

From Ambry Genetics, SCV004988674.1

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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: Oct 13, 2024

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Relating variation to medicine