Variant #0000963093 (NC_000004.11:g.186329171G>T, NM_181726.2:c.*8000G>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.186329171G>T
DNA change (hg38) -
Published as UFSP2(NM_018359.5):c.1040C>A (p.S347*)
ISCN -
DB-ID ANKRD37_000008
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UFSP2 NM_018359.3 ?/. - c.1040C>A r.(?) p.(Ser347*)
ANKRD37 NM_181726.2 ?/. - c.*8000G>T r.(=) p.(=)


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