Variant #0000617485 (NC_000019.9:g.19304942G>A, NM_001145783.1:c.-2016C>T (MEF2BNB))

Chromosome 19
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.19304942G>A
DNA change (hg38) g.19194133G>A
Published as RFXANK(NM_003721.2):c.187G>A (p.A63T)
ISCN -
DB-ID MEF2B_000001 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) 9.0E-5 View details
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEF2BNB NM_001145783.1 ?/. - c.-2016C>T r.(?) p.(=)
MEF2B NM_001145785.1 ?/. - c.-23958C>T r.(?) p.(=)
RFXANK NM_003721.2 ?/. - c.187G>A r.(?) p.(Ala63Thr)
MEF2BNB-MEF2B NM_005919.3 ?/. - c.-2269C>T r.(?) p.(=)
NR2C2AP NM_176880.4 ?/. - c.*7792C>T r.(=) p.(=)


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