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NM_000155.4(GALT):c.919T>A (p.Ser307Thr) AND Galactosemia

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 9, 2017
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV001276335.2

Allele description [Variation Report for NM_000155.4(GALT):c.919T>A (p.Ser307Thr)]

NM_000155.4(GALT):c.919T>A (p.Ser307Thr)

Gene:
GALT:galactose-1-phosphate uridylyltransferase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9p13.3
Genomic location:
Preferred name:
NM_000155.4(GALT):c.919T>A (p.Ser307Thr)
Other names:
p.Ser307Thr
HGVS:
  • NC_000009.12:g.34649424T>A
  • NG_009029.2:g.7836T>A
  • NG_028966.1:g.2240T>A
  • NM_000155.4:c.919T>AMANE SELECT
  • NM_001258332.2:c.592T>A
  • NP_000146.2:p.Ser307Thr
  • NP_001245261.1:p.Ser198Thr
  • NC_000009.11:g.34649421T>A
  • NM_000155.3:c.919T>A
Protein change:
S198T
Links:
dbSNP: rs61735983
NCBI 1000 Genomes Browser:
rs61735983
Molecular consequence:
  • NM_000155.4:c.919T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001258332.2:c.592T>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Galactosemia
Synonyms:
Galactose intolerance
Identifiers:
MONDO: MONDO:0018116; MedGen: C0016952; OMIM: PS230400; Human Phenotype Ontology: HP:0004919

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001462507Natera, Inc.
no assertion criteria provided
Uncertain significance
(May 9, 2017)
germlineclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Natera, Inc., SCV001462507.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024