Variant #0001006701 (NC_000023.10:g.3239545C>A, NM_015419.3:c.4181G>T (MXRA5))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3239545C>A
DNA change (hg38) -
Published as MXRA5(NM_015419.3):c.4181G>T (p.G1394V, p.(Gly1394Val))
ISCN -
DB-ID MXRA5_000110 See all 2 reported entries
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) 1.0E-5 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 2024-08-28 13:16:32 +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     
MXRA5 NM_015419.3 ?/. - c.4181G>T r.(?) p.(Gly1394Val)


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