Variant #0001040954 (NC_000016.9:g.2259410G>A, NM_022372.4:c.*532G>A (MLST8))

Chromosome 16
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.2259410G>A
DNA change (hg38) -
Published as BRICD5(NM_182563.4):c.640C>T (p.(Pro214Ser))
ISCN -
DB-ID MLST8_000006
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) 0.00352 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
PGP NM_001042371.2 -?/. - c.*4319C>T r.(=) p.(=)
MLST8 NM_022372.4 -?/. - c.*532G>A r.(=) p.(=)
BRICD5 NM_182563.3 -?/. - c.640C>T r.(?) p.(Pro214Ser)


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