U.S. flag

An official website of the United States government

NM_000209.4(PDX1):c.8G>C (p.Gly3Ala) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 16, 2022
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:
RCV002493262.3

Allele description [Variation Report for NM_000209.4(PDX1):c.8G>C (p.Gly3Ala)]

NM_000209.4(PDX1):c.8G>C (p.Gly3Ala)

Gene:
PDX1:pancreatic and duodenal homeobox 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q12.2
Genomic location:
Preferred name:
NM_000209.4(PDX1):c.8G>C (p.Gly3Ala)
HGVS:
  • NC_000013.11:g.27920146G>C
  • NG_008183.1:g.5116G>C
  • NM_000209.4:c.8G>CMANE SELECT
  • NP_000200.1:p.Gly3Ala
  • NC_000013.10:g.28494283G>C
  • NC_000013.10:g.28494283G>C
  • NM_000209.3:c.8G>C
Protein change:
G3A
Links:
dbSNP: rs1380564366
NCBI 1000 Genomes Browser:
rs1380564366
Molecular consequence:
  • NM_000209.4:c.8G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Maturity-onset diabetes of the young type 4 (MODY4)
Synonyms:
MODY type 4; Diabetes mellitus MODY type 4; MODY insulin promoter factor-1 related; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0011667; MedGen: C1833382; Orphanet: 552; OMIM: 606392
Name:
Pancreatic agenesis 1 (PAGEN1)
Synonyms:
PANCREATIC HYPOPLASIA, CONGENITAL; Pancreatic agenesis, congenital
Identifiers:
MONDO: MONDO:0024547; MedGen: C3891828; Orphanet: 2805; OMIM: 260370
Name:
Type 2 diabetes mellitus
Synonyms:
DIABETES MELLITUS, TYPE 2, PROTECTION AGAINST; Type II diabetes mellitus; Diabetes mellitus, noninsulin-dependent, late onset
Identifiers:
MONDO: MONDO:0005148; MeSH: D003924; MedGen: C0011860; OMIM: 125853; Human Phenotype Ontology: HP:0005978

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002779206Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Mar 16, 2022) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical 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 Fulgent Genetics, Fulgent Genetics, SCV002779206.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 15, 2024