Variant #0000722263 (NC_000009.11:g.129377658A>G, NC_000009.11(NM_002316.3):c.140-4A>G (LMX1B))

Chromosome 9
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.129377658A>G
DNA change (hg38) -
Published as LMX1B(NM_001174146.2):c.140-4A>G
ISCN -
DB-ID LMX1B_000196 See all 2 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) 0.00043 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 2021-02-08 18:36:18 +01:00 (CET)
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     
LMX1B NM_001174146.1 -?/. - c.140-4A>G r.spl? p.?
LMX1B NM_001174147.1 -?/. - c.140-4A>G r.spl? p.?
LMX1B NM_002316.3 -?/. - c.140-4A>G r.spl? p.?


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