Variant #0000287095 (NC_000009.11:g.35074973C>T, NM_004629.1:c.1587G>A (FANCG))

Chromosome 9
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.35074973C>T
DNA change (hg38) g.35074976C>T
Published as FANCG(NM_004629.1):c.1587G>A (p.Q529=)
ISCN -
DB-ID FANCG_000071
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-25 13:21:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCG NM_004629.1 -?/. - c.1587G>A r.(?) p.(Gln529=) -
VCP NM_007126.3 -?/. - c.-2623G>A r.(?) p.(=) -


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