Variant #0000521217 (NC_000004.11:g.113568916_113568917del, C4orf21(NM_018392.4):c.-10974_-10973del)

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.113568916_113568917del
DNA change (hg38) g.112647760_112647761del
Published as LARP7(NM_001267039.4):c.1068_1069delAA (p.R357Efs*3)
ISCN -
DB-ID C4orf21_000010
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LARP7 NM_016648.2 +/. - c.1068_1069del r.(?) p.(Arg357GlufsTer3)
C4orf21 NM_018392.4 +/. - c.-10974_-10973del r.(?) p.(=)