Variant #0000325450 (NC_000017.10:g.42987562C>T, NC_000017.10(NM_002055.4):c.1171+421G>A (GFAP))

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.42987562C>T
DNA change (hg38) g.44910194C>T
Published as GFAP(NM_001131019.2):c.1238G>A (p.(Arg413Gln)), GFAP(NM_001363846.1):c.1238G>A (p.R413Q)
ISCN -
DB-ID GFAP_000004 See all 2 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) 0.00038 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GFAP NM_002055.4 -?/. - c.1171+421G>A r.(=) p.(=)
CCDC103 NM_213607.2 -?/. - c.*7377C>T r.(=) p.(=)


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