Variant #0000688656 (NC_000002.11:g.220096753_220096755del, NM_024085.3:c.-2524_-2522del (ATG9A))

Chromosome 2
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.220096753_220096755del
DNA change (hg38) -
Published as ANKZF1(NM_018089.3):c.252_254delCCA (p.H84del)
ISCN -
DB-ID ANKZF1_000006
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 2020-09-15 15:50:26 +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     
ANKZF1 NM_018089.2 -?/. - c.252_254del r.(?) p.(His84del)
ATG9A NM_024085.3 -?/. - c.-2524_-2522del r.(?) p.(=)
GLB1L NM_024506.3 -?/. - c.*5043_*5045del r.(=) p.(=)


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