Variant #0000540819 (NC_000010.10:g.75010693G>T, NM_173348.1:c.*9916G>T (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.75010693G>T
DNA change (hg38) g.73250935G>T
Published as -
ISCN -
DB-ID DNAJC9_000003
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) 0 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-3746C>A r.(?) p.(=)
MRPS16 NM_016065.3 +?/. - c.331C>A r.(?) p.(Arg111=)
TTC18 NM_145170.3 +?/. - c.*3040C>A r.(=) p.(=)
FAM149B1 NM_173348.1 +?/. - c.*9916G>T r.(=) p.(=)
DNAJC9-AS1 NR_038373.1 +?/. - n.175+2485G>T r.(?) -


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