Variant #0001006072 (NC_000022.10:g.39911230_39911233dup, NM_019008.4:c.*902_*905dup (SMCR7L))

Chromosome 22
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.39911230_39911233dup
DNA change (hg38) -
Published as MIEF1(NM_019008.4):c.*902_*905dupATCA (p.?)
ISCN -
DB-ID SMCR7L_000004
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     
SMCR7L NM_019008.4 ?/. - c.*902_*905dup r.(=) p.(=)


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