Variant #0001042529 (NC_000018.9:g.77798513G>C, NM_006701.2:c.-50121C>G (TXNL4A))

Chromosome 18
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.77798513G>C
DNA change (hg38) -
Published as RBFA(NM_024805.3):c.387G>C (p.(Leu129=))
ISCN -
DB-ID RBFA_000001
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) 0.00267 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TXNL4A NM_006701.2 -?/. - c.-50121C>G r.(?) p.(=)
RBFA NM_024805.2 -?/. - c.387G>C r.(?) p.(=)


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