Variant #0000720189 (NC_000005.9:g.137222990G>T, NM_006790.2:c.1413G>T (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.137222990G>T
DNA change (hg38) -
Published as MYOT(NM_006790.2):c.1413G>T (p.L471F)
ISCN -
DB-ID MYOT_000017 See all 3 reported entries
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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.-2191G>T r.(?) p.(=)
MYOT NM_006790.2 ?/. - c.1413G>T r.(?) p.(Leu471Phe)
PKD2L2 NM_014386.2 ?/. - c.-2191G>T r.(?) p.(=)
FAM13B NM_016603.2 ?/. - c.*52924C>A r.(=) p.(=)


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