Variant #0000982541 (NC_000017.10:g.42428538G>A, NC_000017.10(NM_002087.2):c.835+7G>A (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.42428538G>A
DNA change (hg38) -
Published as GRN(NM_002087.2):c.835+7G>A, GRN(NM_002087.4):c.835+7G>A
ISCN -
DB-ID FAM171A2_000010 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) 0.04558 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.835+7G>A r.(=) p.(=)
FAM171A2 NM_198475.2 -/. - c.*2563C>T r.(=) p.(=)


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