NM_001370658.1(BTD):c.1177G>A (p.Gly393Ser) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 22, 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:: RCV003480039.1

Allele description [Variation Report for NM_001370658.1(BTD):c.1177G>A (p.Gly393Ser)]

NM_001370658.1(BTD):c.1177G>A (p.Gly393Ser)

Gene:

BTD:biotinidase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.1

Genomic location:

Preferred name:

NM_001370658.1(BTD):c.1177G>A (p.Gly393Ser)

Other names:

G413S; p.Gly413Ser

HGVS:

NC_000003.12:g.15645093G>A
NG_008019.2:g.48742G>A
NG_008019.3:g.48743G>A
NM_000060.4:c.1237G>A
NM_001281723.4:c.1177G>A
NM_001281724.3:c.1177G>A
NM_001281725.3:c.1177G>A
NM_001323582.2:c.1177G>A
NM_001370658.1:c.1177G>AMANE SELECT
NM_001370752.1:c.1015+162G>A
NM_001370753.1:c.399+3036G>A
NM_001407364.1:c.1177G>A
NM_001407365.1:c.1177G>A
NM_001407366.1:c.1177G>A
NM_001407367.1:c.1177G>A
NM_001407368.1:c.1177G>A
NM_001407369.1:c.1177G>A
NM_001407370.1:c.1177G>A
NM_001407371.1:c.1177G>A
NM_001407372.1:c.1177G>A
NM_001407373.1:c.1177G>A
NM_001407374.1:c.1177G>A
NM_001407375.1:c.1177G>A
NM_001407376.1:c.1177G>A
NM_001407377.1:c.1177G>A
NM_001407378.1:c.1177G>A
NP_000051.1:p.Gly413Ser
NP_001268652.2:p.Gly393Ser
NP_001268652.2:p.Gly393Ser
NP_001268653.2:p.Gly393Ser
NP_001268654.1:p.Gly393Ser
NP_001268654.1:p.Gly393Ser
NP_001310511.1:p.Gly393Ser
NP_001310511.1:p.Gly393Ser
NP_001357587.1:p.Gly393Ser
NP_001394293.1:p.Gly393Ser
NP_001394294.1:p.Gly393Ser
NP_001394295.1:p.Gly393Ser
NP_001394296.1:p.Gly393Ser
NP_001394297.1:p.Gly393Ser
NP_001394298.1:p.Gly393Ser
NP_001394299.1:p.Gly393Ser
NP_001394300.1:p.Gly393Ser
NP_001394301.1:p.Gly393Ser
NP_001394302.1:p.Gly393Ser
NP_001394303.1:p.Gly393Ser
NP_001394304.1:p.Gly393Ser
NP_001394305.1:p.Gly393Ser
NP_001394306.1:p.Gly393Ser
NP_001394307.1:p.Gly393Ser
NC_000003.11:g.15686600G>A
NM_001281723.3:c.1177G>A
NM_001281725.2:c.1177G>A
NM_001323582.1:c.1177G>A

Protein change:

G393S

Links:

dbSNP: rs374141881

NCBI 1000 Genomes Browser:

rs374141881

Molecular consequence:

NM_001370752.1:c.1015+162G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370753.1:c.399+3036G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_000060.4:c.1237G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281723.4:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281724.3:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001281725.3:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001323582.2:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001370658.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407364.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407365.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407366.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407367.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407368.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407369.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407370.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407371.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407372.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407373.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407374.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407375.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407376.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407377.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001407378.1:c.1177G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004226053	Mayo Clinic Laboratories, Mayo Clinic	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Dec 22, 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

SCV004226053

Mayo Clinic Laboratories, Mayo Clinic

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Dec 22, 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	1	not provided	not provided	not provided	not provided	clinical 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 Mayo Clinic Laboratories, Mayo Clinic, SCV004226053.1

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

Description

PP3, PM2

#	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		1	not provided	not provided	not provided

Last Updated: Oct 8, 2024

ClinVar

Relating variation to medicine