Variant #0000561957 (NC_000017.10:g.42979917A>C, NM_002055.4:c.*4798T>G (GFAP))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42979917A>C
DNA change (hg38) g.44902549A>C
Published as CCDC103(NM_001258395.1):c.461A>C (p.(His154Pro)), CCDC103(NM_213607.3):c.461A>C (p.H154P)
ISCN -
DB-ID CCDC103_000001 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) 0.00122 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.*4798T>G r.(=) p.(=)
EFTUD2 NM_004247.3 +/. - c.-3185T>G r.(?) p.(=)
CCDC103 NM_213607.2 +/. - c.461A>C r.(?) p.(His154Pro)


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