Variant #0000678644 (NC_000009.11:g.19050394C>G, NM_153707.2:c.-17488G>C (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.19050394C>G
DNA change (hg38) -
Published as RRAGA(NM_006570.5):c.737C>G (p.A246G)
ISCN -
DB-ID FAM154A_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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRAGA NM_006570.4 ?/. - c.737C>G r.(?) p.(Ala246Gly)
HAUS6 NM_017645.4 ?/. - c.*5947G>C r.(=) p.(=)
FAM154A NM_153707.2 ?/. - c.-17488G>C r.(?) p.(=)


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