Variant #0000575062 (NC_000023.10:g.15544185C>T, NM_003662.3:c.-32959G>A (PIR))

Chromosome X
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.15544185C>T
DNA change (hg38) g.15526062C>T
Published as BMX(NM_001721.6):c.851C>T (p.(Ser284Leu))
ISCN -
DB-ID BMX_000024 See all 2 reported entries
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) 0.00134 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMX NM_001721.6 -?/. - c.851C>T r.(?) p.(Ser284Leu)
PIR NM_003662.3 -?/. - c.-32959G>A r.(?) p.(=)


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