Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect

Exon

DNA change (cDNA)

RNA change

Protein

P-domain

Allele

Classification method

Clinical classification

DNA change (genomic) (hg19)

DNA change (hg38)

Published as

ISCN

DB-ID

Variant remarks

Reference

ClinVar ID

dbSNP ID

Origin

Segregation

Frequency

Re-site

VIP

Methylation

Template

Technique

Tissue

Remarks

Disease

ID_report

Reference

Remarks

Gender

Consanguinity

Country

Population

Age at death

VIP

Data_av

Treatment

Panel size

Owner
+?/. - c.3648C>A r.(?) p.(Tyr1216*) - Parent #1 - likely pathogenic g.216373132G>T g.216199790G>T - - USH2A_002033 - PubMed: Neuhaus 2017 - - Germline yes - - - - DNA MLPA, SEQ - - USH Pat71 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+/. - c.3648C>A r.(?) p.(Tyr1216Ter) - Unknown ACMG pathogenic g.216373132G>T g.216199790G>T - - USH2A_002033 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Neuhaus, C. et al., 2017 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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