Variant #0000559998 (NC_000016.9:g.89883000G>C, NM_000135.2:c.24C>G (FANCA))

Chromosome 16
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.89883000G>C
DNA change (hg38) g.89816592G>C
Published as FANCA(NM_000135.4):c.24C>G (p.N8K)
ISCN -
DB-ID FANCA_000021 See all 6 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) 0.00491 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +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     
FANCA NM_000135.2 -/. - c.24C>G r.(?) p.(Asn8Lys) -
ZNF276 NM_152287.3 -/. - c.*78346G>C r.(=) p.(=) -


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