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NM_000518.5(HBB):c.391T>G (p.Tyr131Asp)

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Interpretation:
other​

Review status:
no assertion criteria provided
Submissions:
1 (Most recent: Jul 20, 2016)
Last evaluated:
Dec 12, 2017
Accession:
VCV000015388.2
Variation ID:
15388
Description:
single nucleotide variant
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NM_000518.5(HBB):c.391T>G (p.Tyr131Asp)

Allele ID
30427
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
11p15.4
Genomic location
11: 5225651 (GRCh38) GRCh38 UCSC
11: 5246881 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
P68871:p.Tyr131Asp
NC_000011.10:g.5225651A>C
NC_000011.9:g.5246881A>C
... more HGVS
Protein change
Y131D
Other names
Y130D
Canonical SPDI
NC_000011.10:5225650:A:C
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
-
Links
ClinGen: CA125233
UniProtKB: P68871#VAR_003063
OMIM: 141900.0297
dbSNP: rs35834416
VarSome
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Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
HEMOGLOBIN WIEN
other 1 no assertion criteria provided Dec 12, 2017 RCV000016641.5
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Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
HBB - - GRCh38
GRCh37
45 1290
LOC107133510 - - - GRCh38 - 1223
LOC110006319 - - - GRCh38 - 573

Submitted interpretations and evidence

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Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter Supporting information
other
(Dec 12, 2017)
no assertion criteria provided
Method: literature only
HEMOGLOBIN WIEN
Allele origin: germline
OMIM
Accession: SCV000036910.5
Submitted: (Jul 20, 2016)
Evidence details
Publications
PubMed (2)

Functional evidence

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There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for this variant

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Title Author Journal Year Link
Structure of haemoglobin Wien beta 130 (H8) tyrosine-aspartic acid: an unstable haemoglobin variant. Lorkin PA Acta haematologica 1974 PMID: 4212355
Molecular pathology of human haemoglobin. Perutz MF Nature 1968 PMID: 5691676

Text-mined citations for rs35834416...

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These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Sep 29, 2021