Variant #0000677401 (NC_000005.9:g.137222898T>A, NC_000005.9(NM_006790.2):c.1325-4T>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.137222898T>A
DNA change (hg38) -
Published as MYOT(NM_006790.2):c.1325-4T>A
ISCN -
DB-ID MYOT_000073
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) 6.0E-5 View details
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.-2283T>A r.(?) p.(=)
MYOT NM_006790.2 -?/. - c.1325-4T>A r.spl? p.?
PKD2L2 NM_014386.2 -?/. - c.-2283T>A r.(?) p.(=)
FAM13B NM_016603.2 -?/. - c.*53016A>T r.(=) p.(=)


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