Variant #0001035803 (NC_000006.11:g.44103069C>T, NM_018426.1:c.244C>T (TMEM63B))

Chromosome 6
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.44103069C>T
DNA change (hg38) -
Published as TMEM63B(NM_018426.3):c.244C>T (p.(Arg82Trp))
ISCN -
DB-ID MRPL14_000008
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) 0.00016 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     
TMEM63B NM_018426.1 -?/. - c.244C>T r.(?) p.(Arg82Trp)
MRPL14 NM_032111.2 -?/. - c.-8007G>A r.(?) p.(=)


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