Variant #0000865309 (NC_000017.10:g.42428176A>T, NC_000017.10(NM_002087.2):c.708+8A>T (GRN))

Chromosome 17
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.42428176A>T
DNA change (hg38) -
Published as GRN(NM_002087.2):c.708+8A>T
ISCN -
DB-ID FAM171A2_000025
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) 0.00014 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.708+8A>T r.(=) p.(=)
FAM171A2 NM_198475.2 -?/. - c.*2925T>A r.(=) p.(=)


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