Variant #0001052107 (NC_000005.9:g.137226266G>A, NM_006790.2:c.*3192G>A (MYOT))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.137226266G>A
DNA change (hg38) -
Published as PKD2L2(NM_001300921.2):c.128G>A (p.(Cys43Tyr))
ISCN -
DB-ID MYOT_000081
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00054 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKD2L2 NM_001300921.1 ?/. - c.128G>A r.(?) p.(Cys43Tyr)
MYOT NM_006790.2 ?/. - c.*3192G>A r.(=) p.(=)
FAM13B NM_016603.2 ?/. - c.*49648C>T r.(=) p.(=)


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