Variant #0000990542 (NC_000001.10:g.169346081G>C, NM_013330.3:c.-9133C>G (NME7))

Chromosome 1
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.169346081G>C
DNA change (hg38) -
Published as BLZF1(NM_003666.2):c.332G>C (p.(Gly111Ala))
ISCN -
DB-ID BLZF1_000002
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) 0.00021 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 2024-08-28 13:07:21 +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     
BLZF1 NM_003666.2 -?/. - c.332G>C r.(?) p.(Gly111Ala)
NME7 NM_013330.3 -?/. - c.-9133C>G r.(?) p.(=)
C1orf114 NM_021179.1 -?/. - c.*18204C>G r.(=) p.(=)


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