Variant #0000657321 (NC_000013.10:g.99947493T>C, NC_000013.10(NM_177967.3):c.285-18858T>C (UBAC2))

Chromosome 13
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.99947493T>C
DNA change (hg38) g.99295239T>C
Published as GPR183(NM_004951.5):c.907A>G (p.M303V)
ISCN -
DB-ID UBAC2_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR18 NM_001098200.1 ?/. - c.-37120A>G r.(?) p.(=)
GPR183 NM_004951.4 ?/. - c.907A>G r.(?) p.(Met303Val)
UBAC2 NM_177967.3 ?/. - c.285-18858T>C r.(=) p.(=)


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