Variant #0000615675 (NC_000016.9:g.1021033_1021051dup, NM_022773.2:c.-39_-21dup (LMF1))

Chromosome 16
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.1021033_1021051dup
DNA change (hg38) g.971033_971051dup
Published as LMF1(NM_001352018.2):c.-362+10126_-362+10144dupAGAATGGGCGGGGCCTCCG
ISCN -
DB-ID LMF1_000303
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 2019-12-04 15:24:38 +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     
LMF1 NM_022773.2 -?/. - c.-39_-21dup r.(?) p.(=)


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