Variant #0000263710 (NC_000015.9:g.91306241G>A, NM_000057.2:c.1928G>A (BLM))

Chromosome 15
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.91306241G>A
DNA change (hg38) g.90763011G>A
Published as BLM(NM_000057.2):c.1928G>A (p.R643H), BLM(NM_000057.4):c.1928G>A (p.R643H), BLM(NM_001287248.1):c.803G>A (p.R268H)
ISCN -
DB-ID BLM_000028 See all 7 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) 0.00323 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLM NM_000057.2 -?/. - c.1928G>A r.(?) p.(Arg643His)


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