Variant #0000334913 (NC_000023.10:g.100749016_100749017insAGGCTC, ARMCX4(NM_001256155.1):c.5440_5441insAGGCTC)

Chromosome X
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.100749016_100749017insAGGCTC
DNA change (hg38) g.101494029_101494030insAGGCTC
Published as ARMCX4(NM_001256155.1):c.5440_5441insAGGCTC (p.(Gly1814delinsGluAlaArg))
ISCN -
DB-ID ARMCX4_000014
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARMCX4 NM_001256155.1 -?/. - c.5440_5441insAGGCTC r.(?) p.(Gly1814delinsGluAlaArg)