Variant #0001063967 (NC_000003.11:g.49054045C>T, NM_177938.2:c.*9705C>T (P4HTM))

Chromosome 3
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.49054045C>T
DNA change (hg38) -
Published as DALRD3(NM_001009996.3):c.1063G>A (p.(Asp355Asn))
ISCN -
DB-ID chr3_007479
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DALRD3 NM_001009996.2 ?/. - c.1063G>A r.(?) p.(Asp355Asn)
WDR6 NM_018031.3 ?/. - c.*1324C>T r.(=) p.(=)
P4HTM NM_177938.2 ?/. - c.*9705C>T r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.-5533C>T r.(?) p.(=)


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