Variant #0000332583 (NC_000009.11:g.19049767G>T, NM_153707.2:c.-16861C>A (FAM154A))

Chromosome 9
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.19049767G>T
DNA change (hg38) g.19049769G>T
Published as RRAGA(NM_006570.4):c.110G>T (p.(Arg37Leu))
ISCN -
DB-ID RRAGA_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRAGA NM_006570.4 ?/. - c.110G>T r.(?) p.(Arg37Leu)
HAUS6 NM_017645.4 ?/. - c.*6574C>A r.(=) p.(=)
FAM154A NM_153707.2 ?/. - c.-16861C>A r.(?) p.(=)


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