Variant #0000925806 (NC_000013.10:g.35738605G>T, NM_005584.4:c.*310591C>A (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.35738605G>T
DNA change (hg38) -
Published as NBEA(NM_015678.5):c.4192G>T (p.G1398*)
ISCN -
DB-ID NBEA_000076
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 2023-04-16 21:50:28 +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     
MAB21L1 NM_005584.4 +/. - c.*310591C>A r.(=) p.(=)
NBEA NM_015678.4 +/. - c.4192G>T r.(?) p.(Gly1398*)


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