Variant #0000614637 (NC_000013.10:g.35751209A>G, NM_005584.4:c.*297987T>C (MAB21L1))

Chromosome 13
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.35751209A>G
DNA change (hg38) g.35177072A>G
Published as NBEA(NM_015678.5):c.4631A>G (p.N1544S)
ISCN -
DB-ID NBEA_000028
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) 9.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAB21L1 NM_005584.4 ?/. - c.*297987T>C r.(=) p.(=)
NBEA NM_015678.4 ?/. - c.4631A>G r.(?) p.(Asn1544Ser)


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