Variant #0000990212 (NC_000001.10:g.1289293A>T, NM_004421.2:c.-4848T>A (DVL1))

Chromosome 1
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.1289293A>T
DNA change (hg38) -
Published as MXRA8(NM_001282585.1):c.1256T>A (p.(Ile413Asn))
ISCN -
DB-ID MXRA8_000001 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) Retrieve
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 13:07:21 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DVL1 NM_004421.2 ?/. - c.-4848T>A r.(?) p.(=)
MXRA8 NM_032348.2 ?/. - c.1238T>A r.(?) p.(Ile413Asn)


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