Variant #0000678667 (NC_000009.11:g.35075969G>A, NM_004629.1:c.1133C>T (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.35075969G>A
DNA change (hg38) -
Published as FANCG(NM_004629.1):c.1133C>T (p.(Ser378Leu)), FANCG(NM_004629.2):c.1133C>T (p.S378L)
ISCN -
DB-ID FANCG_000073 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) 0.00768 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCG NM_004629.1 -?/. - c.1133C>T r.(?) p.(Ser378Leu) -
VCP NM_007126.3 -?/. - c.-3619C>T r.(?) p.(=) -


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