Variant #0000254884 (NC_000017.10:g.42426916A>G, NM_002087.2:c.261A>G (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.42426916A>G
DNA change (hg38) g.44349548A>G
Published as GRN(NM_002087.2):c.261A>G (p.P87=)
ISCN -
DB-ID GRN_000155
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 16:41:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRN NM_002087.2 -?/. - c.261A>G r.(?) p.(Pro87=)
FAM171A2 NM_198475.2 -?/. - c.*4185T>C r.(=) p.(=)


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