Variant #0000612631 (NC_000010.10:g.75011557del, NM_173348.1:c.*10780del (FAM149B1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.75011557del
DNA change (hg38) g.73251799del
Published as -
ISCN -
DB-ID DNAJC9_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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +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     
DNAJC9 NM_015190.3 +?/. - c.-4607del r.(?) p.(=)
MRPS16 NM_016065.3 +?/. - c.241del r.(?) p.(Ala81ProfsTer22)
TTC18 NM_145170.3 +?/. - c.*2179del r.(?) p.(=)
FAM149B1 NM_173348.1 +?/. - c.*10780del r.(?) p.(=)
DNAJC9-AS1 NR_038373.1 +?/. - n.175+3349del r.(?) -


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