Variant #0001064907 (NC_000008.10:g.37620224_37620225dup, NM_007198.3:c.47_48dup (PROSC))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37620224_37620225dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID ERLIN2_000019
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERLIN2 NM_007175.6 +/. - c.*8591_*8592dup r.(=) p.(=)
PROSC NM_007198.3 +/. - c.47_48dup r.(?) p.(Leu17Hisfs*5)


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