Variant #0000556232 (NC_000015.9:g.91310214A>G, NM_000057.2:c.2268A>G (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.91310214A>G
DNA change (hg38) g.90766984A>G
Published as BLM(NM_000057.2):c.2268A>G (p.K756=), BLM(NM_000057.4):c.2268A>G (p.K756=), BLM(NM_001287248.1):c.1143A>G (p.K381=)
ISCN -
DB-ID BLM_000058 See all 4 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) 0.00187 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.2268A>G r.(?) p.(Lys756=)


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