Variant #0000609500 (NC_000005.9:g.137226177G>A, NM_006790.2:c.*3103G>A (MYOT))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.137226177G>A
DNA change (hg38) g.137890488G>A
Published as PKD2L2(NM_001258449.1):c.39G>A (p.S13=)
ISCN -
DB-ID MYOT_000066
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKD2L2 NM_001300921.1 -?/. - c.39G>A r.(?) p.(Ser13=)
MYOT NM_006790.2 -?/. - c.*3103G>A r.(=) p.(=)
PKD2L2 NM_014386.2 -?/. - c.39G>A r.(?) p.(Ser13=)
FAM13B NM_016603.2 -?/. - c.*49737C>T r.(=) p.(=)


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