Variant #0000561924 (NC_000017.10:g.42428954G>A, NM_002087.2:c.970G>A (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.42428954G>A
DNA change (hg38) g.44351586G>A
Published as GRN(NM_002087.2):c.970G>A (p.A324T), GRN(NM_002087.4):c.970G>A (p.A324T)
ISCN -
DB-ID GRN_000038 See all 4 reported entries
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) 0.00086 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRN NM_002087.2 -?/. - c.970G>A r.(?) p.(Ala324Thr)
FAM171A2 NM_198475.2 -?/. - c.*2147C>T r.(=) p.(=)


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