Variant #0001024913 (NC_000004.11:g.186283133A>G, NM_181726.2:c.-34945A>G (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.186283133A>G
DNA change (hg38) -
Published as SNX25(NM_001317781.2):c.2215A>G (p.I739V)
ISCN -
DB-ID ANKRD37_000016
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) 0.00017 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +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     
LRP2BP NM_018409.3 ?/. - c.*5201T>C r.(=) p.(=)
SNX25 NM_031953.2 ?/. - c.2215A>G r.(?) p.(Ile739Val)
ANKRD37 NM_181726.2 ?/. - c.-34945A>G r.(?) p.(=)


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