Variant #0000658533 (NC_000019.9:g.19431689_19431700del, NM_015329.3:c.21_32del (MAU2))

Chromosome 19
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.19431689_19431700del
DNA change (hg38) g.19320880_19320891del
Published as MAU2(NM_015329.4):c.21_32delAGCGGCCCAGGC (p.Q10_A13del)
ISCN -
DB-ID MAU2_000004
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAU2 NM_015329.3 -?/. - c.21_32del r.(?) p.(Gln10_Ala13del)
SUGP1 NM_172231.3 -?/. - c.-392_-381del r.(?) p.(=)


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