Variant #0000266522 (NC_000017.10:g.42979670C>A, NM_002055.4:c.*5045G>T (GFAP))

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.42979670C>A
DNA change (hg38) g.44902302C>A
Published as CCDC103(NM_001258397.3):c.277-16C>A
ISCN -
DB-ID CCDC103_000003
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) 0.26865 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*5045G>T r.(=) p.(=)
EFTUD2 NM_004247.3 -/. - c.-2938G>T r.(?) p.(=)
CCDC103 NM_213607.2 -/. - c.277-63C>A r.(=) p.(=)


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