Variant #0000982543 (NC_000017.10:g.42430144del, NM_002087.2:c.1760del (GRN))

Chromosome 17
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.42430144del
DNA change (hg38) -
Published as GRN(NM_002087.4):c.1760del (p.(Pro587Glnfs*3))
ISCN -
DB-ID FAM171A2_000030
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 2024-04-19 20:27:30 +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     
GRN NM_002087.2 ?/. - c.1760del r.(?) p.(Pro587Glnfs*3)
FAM171A2 NM_198475.2 ?/. - c.*959del r.(?) p.(=)


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