Variant #0001063966 (NC_000003.11:g.49053230T>C, NM_177938.2:c.*8890T>C (P4HTM))

Chromosome 3
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.49053230T>C
DNA change (hg38) -
Published as DALRD3(NM_001009996.3):c.1512+7A>G
ISCN -
DB-ID chr3_007478
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.1512+7A>G r.(=) p.(=)
WDR6 NM_018031.3 -?/. - c.*509T>C r.(=) p.(=)
P4HTM NM_177938.2 -?/. - c.*8890T>C r.(=) p.(=)
NDUFAF3 NM_199069.1 -?/. - c.-6348T>C r.(?) p.(=)


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