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NM_000518.4(HBB):c.299A>C (p.Asp100Ala) AND Erythrocytosis, familial, 6

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jan 1, 1964
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:
RCV000641589.1

Allele description [Variation Report for NM_000518.4(HBB):c.299A>C (p.Asp100Ala)]

NM_000518.4(HBB):c.299A>C (p.Asp100Ala)

Genes:
LOC106099062:HBB recombination region [Gene]
HBB:hemoglobin subunit beta [Gene - OMIM - HGNC]
LOC107133510:origin of replication at HBB [Gene]
Variant type:
single nucleotide variant
Cytogenetic location:
11p15.4
Genomic location:
Preferred name:
NM_000518.4(HBB):c.299A>C (p.Asp100Ala)
Other names:
D99A
HGVS:
  • NC_000011.10:g.5226593T>G
  • NG_000007.3:g.71023A>C
  • NG_042296.1:g.124T>G
  • NG_046672.1:g.4528T>G
  • NG_053049.1:g.2914T>G
  • NG_059281.1:g.5479A>C
  • NM_000518.5:c.299A>CMANE SELECT
  • NP_000509.1:p.Asp100Ala
  • LRG_1232t1:c.299A>C
  • LRG_1232:g.5479A>C
  • LRG_1232p1:p.Asp100Ala
  • NC_000011.9:g.5247823T>G
Protein change:
D100A; ASP99ALA
Links:
HBVAR: 454; OMIM: 141900.0230; dbSNP: rs33971048
NCBI 1000 Genomes Browser:
rs33971048
Molecular consequence:
  • NM_000518.5:c.299A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Erythrocytosis, familial, 6
Synonyms:
ERYTHROCYTOSIS, BETA-GLOBIN TYPE; POLYCYTHEMIA, BETA-GLOBIN TYPE
Identifiers:
MONDO: MONDO:0054801; MedGen: C4693822; OMIM: 617980

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000763231OMIM
no assertion criteria provided
Pathogenic
(Jan 1, 1964)
germlineliterature only

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot providednot providednot providednot providednot providednot providedliterature only

Citations

PubMed

HEMOGLOBIN J (BALTIMORE) COEXISTING IN A FAMILY WITH HEMOGLOBIN S.

WEATHERALL DJ.

Bull Johns Hopkins Hosp. 1964 Jan;114:1-12. No abstract available.

PubMed [citation]
PMID:
14117783

Details of each submission

From OMIM, SCV000763231.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedliterature only PubMed (1)

Description

Cause of polycythemia. See Weatherall et al. (1977).

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 23, 2022