Variant #0000690770 (NC_000010.10:g.75010692C>T, NM_173348.1:c.*9915C>T (FAM149B1))

Chromosome 10
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.75010692C>T
DNA change (hg38) -
Published as MRPS16(NM_016065.3):c.332G>A (p.R111Q)
ISCN -
DB-ID DNAJC9_000005
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
DNAJC9 NM_015190.3 ?/. - c.-3745G>A r.(?) p.(=)
MRPS16 NM_016065.3 ?/. - c.332G>A r.(?) p.(Arg111Gln)
TTC18 NM_145170.3 ?/. - c.*3041G>A r.(=) p.(=)
FAM149B1 NM_173348.1 ?/. - c.*9915C>T r.(=) p.(=)
DNAJC9-AS1 NR_038373.1 ?/. - n.175+2484C>T r.(?) -


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