Variant #0000994233 (NC_000004.11:g.186336474A>C, NM_181726.2:c.*15303A>C (ANKRD37))

Chromosome 4
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.186336474A>C
DNA change (hg38) -
Published as UFSP2(NM_018359.3):c.519T>G (p.(Ile173Met))
ISCN -
DB-ID ANKRD37_000015
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UFSP2 NM_018359.3 -?/. - c.519T>G r.(?) p.(Ile173Met)
ANKRD37 NM_181726.2 -?/. - c.*15303A>C r.(=) p.(=)


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