Variant #0000894891 (NC_000019.9:g.19308014C>T, NM_001145783.1:c.-5088G>A (MEF2BNB))

Chromosome 19
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.19308014C>T
DNA change (hg38) -
Published as RFXANK(NM_003721.2):c.291C>T (p.L97=)
ISCN -
DB-ID MEF2B_000005
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +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     
MEF2BNB NM_001145783.1 -?/. - c.-5088G>A r.(?) p.(=)
MEF2B NM_001145785.1 -?/. - c.-27030G>A r.(?) p.(=)
RFXANK NM_003721.2 -?/. - c.291C>T r.(?) p.(Leu97=)
MEF2BNB-MEF2B NM_005919.3 -?/. - c.-5341G>A r.(?) p.(=)
NR2C2AP NM_176880.4 -?/. - c.*4720G>A r.(=) p.(=)


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