Variant #0001051890 (NC_000004.11:g.186298078T>C, NM_181726.2:c.-20000T>C (ANKRD37))

Chromosome 4
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.186298078T>C
DNA change (hg38) -
Published as LRP2BP(NM_001377440.1):c.201A>G (p.(Gln67=))
ISCN -
DB-ID ANKRD37_000017
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) 0.00012 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRP2BP NM_018409.3 ?/. - c.201A>G r.(?) p.(=)
SNX25 NM_031953.2 ?/. - c.*13459T>C r.(=) p.(=)
ANKRD37 NM_181726.2 ?/. - c.-20000T>C r.(?) p.(=)


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