Variant #0000559963 (NC_000016.9:g.89805301G>C, NM_000135.2:c.4249C>G (FANCA))

Chromosome 16
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.89805301G>C
DNA change (hg38) g.89738893G>C
Published as FANCA(NM_000135.2):c.4249C>G (p.(His1417Asp), p.H1417D), FANCA(NM_000135.4):c.4249C>G (p.H1417D), FANCA(NM_001286167.2):c.4253C>G (p.T1418R)
ISCN -
DB-ID FANCA_000311 See all 11 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) 0.00353 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.4249C>G r.(?) p.(His1417Asp) -
VPS9D1 NM_004913.2 -?/. - c.-18032C>G r.(?) p.(=) -
ZNF276 NM_152287.3 -?/. - c.*647G>C r.(=) p.(=) -


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