Variant #0000550719 (NC_000013.10:g.35733981_35733982del, NM_005584.4:c.*315214_*315215del (MAB21L1))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35733981_35733982del
DNA change (hg38) g.35159844_35159845del
Published as NBEA(NM_015678.4):c.3673_3674delTT (p.L1225Sfs*5)
ISCN -
DB-ID NBEA_000016
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-03 16:23:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAB21L1 NM_005584.4 +/. - c.*315214_*315215del r.(=) p.(=)
NBEA NM_015678.4 +/. - c.3673_3674del r.(?) p.(Leu1225SerfsTer5)


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