Variant #0000690257 (NC_000008.10:g.37690592G>C, NM_018310.3:c.*11416C>G (BRF2))

Chromosome 8
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.37690592G>C
DNA change (hg38) -
Published as ADGRA2(NM_032777.9):c.1162G>C (p.V388L)
ISCN -
DB-ID BRF2_000004
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 2020-09-15 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     
BRF2 NM_018310.3 -?/. - c.*11416C>G r.(=) p.(=)
GPR124 NM_032777.9 -?/. - c.1162G>C r.(?) p.(Val388Leu)


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