Variant #0000283399 (NC_000017.10:g.42427630T>C, NM_002087.2:c.384T>C (GRN))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42427630T>C
DNA change (hg38) g.44350262T>C
Published as GRN(NM_002087.2):c.384T>C (p.D128=), GRN(NM_002087.4):c.384T>C (p.(Asp128=), p.D128=)
ISCN -
DB-ID GRN_000020 See all 6 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) 0.0507 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.384T>C r.(?) p.(Asp128=)
FAM171A2 NM_198475.2 -/. - c.*3471A>G r.(=) p.(=)


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