Variant #0000892491 (NC_000016.9:g.1030987G>A, NM_022773.2:c.-10007C>T (LMF1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1030987G>A
DNA change (hg38) -
Published as LMF1(NM_001352018.2):c.-362+158C>T
ISCN -
DB-ID LMF1_000558
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX8 NM_014587.3 -/. - c.-936G>A r.(?) p.(=)
LMF1 NM_022773.2 -/. - c.-10007C>T r.(?) p.(=)


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