Variant #0000251636 (NC_000019.9:g.19310047A>G, NM_001145783.1:c.-7121T>C (MEF2BNB))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19310047A>G
DNA change (hg38) g.19199238A>G
Published as RFXANK(NM_003721.2):c.712+4A>G
ISCN -
DB-ID RFXANK_000002
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) 0.00737 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 2018-01-15 20:58:59 +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.-7121T>C r.(?) p.(=)
RFXANK NM_003721.2 -/. - c.712+4A>G r.spl? p.?
MEF2BNB-MEF2B NM_005919.3 -/. - c.-7374T>C r.(?) p.(=)
NR2C2AP NM_176880.4 -/. - c.*2687T>C r.(=) p.(=)


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