Variant #0000263725 (NC_000001.10:g.169347732G>C, NM_013330.3:c.-10784C>G (NME7))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.169347732G>C
DNA change (hg38) g.169378494G>C
Published as BLZF1(NM_003666.3):c.633G>C (p.Q211H)
ISCN -
DB-ID BLZF1_000001
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) 5.0E-5 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 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     
BLZF1 NM_003666.2 ?/. - c.633G>C r.(?) p.(Gln211His)
NME7 NM_013330.3 ?/. - c.-10784C>G r.(?) p.(=)
C1orf114 NM_021179.1 ?/. - c.*16553C>G r.(=) p.(=)


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