Variant #0000994230 (NC_000004.11:g.186283113A>T, NM_181726.2:c.-34965A>T (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.186283113A>T
DNA change (hg38) -
Published as SNX25(NM_031953.2):c.2195A>T (p.(Glu732Val))
ISCN -
DB-ID ANKRD37_000012
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 13:16:32 +02:00 (CEST)
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.*5221T>A r.(=) p.(=)
SNX25 NM_031953.2 ?/. - c.2195A>T r.(?) p.(Glu732Val)
ANKRD37 NM_181726.2 ?/. - c.-34965A>T r.(?) p.(=)


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