Variant #0000677400 (NC_000005.9:g.137221896G>A, NM_006790.2:c.1184G>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.137221896G>A
DNA change (hg38) -
Published as MYOT(NM_006790.2):c.1184G>A (p.R395Q)
ISCN -
DB-ID MYOT_000072
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.-3285G>A r.(?) p.(=)
MYOT NM_006790.2 ?/. - c.1184G>A r.(?) p.(Arg395Gln)
PKD2L2 NM_014386.2 ?/. - c.-3285G>A r.(?) p.(=)
FAM13B NM_016603.2 ?/. - c.*54018C>T r.(=) p.(=)


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