Variant #0000893959 (NC_000017.10:g.42429557_42429577del, NM_002087.2:c.1354_1374del (GRN))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.42429557_42429577del
DNA change (hg38) -
Published as GRN(NM_002087.4):c.1354_1374delGTGGGGCAGACCTGCTGCCCG (p.V452_P458del)
ISCN -
DB-ID FAM171A2_000027
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.1354_1374del r.(?) p.(Val452_Pro458del)
FAM171A2 NM_198475.2 ?/. - c.*1532_*1552del r.(=) p.(=)


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