Variant #0000866946 (NC_000023.10:g.103267293_103267294del, NM_001002916.3:c.521_522del (H2BFWT))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.103267293_103267294del
DNA change (hg38) -
Published as H2BFWT(NM_001002916.4):c.521_522delGA (p.R174Kfs*20)
ISCN -
DB-ID H2BFWT_000012
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
H2BFWT NM_001002916.3 ?/. - c.521_522del r.(?) p.(Arg174Lysfs*20)


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