Variant #0000561960 (NC_000017.10:g.42985442C>T, NM_002055.4:c.1247G>A (GFAP))

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.42985442C>T
DNA change (hg38) g.44908074C>T
Published as GFAP(NM_001131019.2):c.*2062G>A (p.(=)), GFAP(NM_002055.4):c.1247G>A (p.R416Q)
ISCN -
DB-ID GFAP_000001 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) 9.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.1247G>A r.(?) p.(Arg416Gln)
CCDC103 NM_213607.2 ?/. - c.*5257C>T r.(=) p.(=)


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