Variant #0000323453 (NC_000013.10:g.99948315T>C, NC_000013.10(NM_177967.3):c.285-18036T>C (UBAC2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.99948315T>C
DNA change (hg38) g.99296061T>C
Published as GPR183(NM_004951.4):c.85A>G (p.(Thr29Ala))
ISCN -
DB-ID UBAC2_000002
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR18 NM_001098200.1 -?/. - c.-37942A>G r.(?) p.(=)
GPR183 NM_004951.4 -?/. - c.85A>G r.(?) p.(Thr29Ala)
UBAC2 NM_177967.3 -?/. - c.285-18036T>C r.(=) p.(=)


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