Variant #0000572555 (NC_000023.10:g.100531437_100531442del, NM_024885.3:c.1047_1052del (TAF7L))

Chromosome X
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.100531437_100531442del
DNA change (hg38) g.101276449_101276454del
Published as TAF7L(NM_024885.4):c.1047_1052delGGATGA (p.E353_D354del)
ISCN -
DB-ID TAF7L_000045
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF7L NM_024885.3 -/. - c.1047_1052del r.(?) p.(Glu353_Asp354del)


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