Variant #0000561923 (NC_000017.10:g.42428929_42428930del, NM_002087.2:c.945_946del (GRN))

Chromosome 17
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.42428929_42428930del
DNA change (hg38) g.44351561_44351562del
Published as GRN(NM_002087.2):c.945_946delTG (p.C315*)
ISCN -
DB-ID FAM171A2_000014
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-13 16:50:53 +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.945_946del r.(?) p.(Cys315Ter)
FAM171A2 NM_198475.2 +/. - c.*2173_*2174del r.(=) p.(=)


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