Variant #0000949187 (NC_000009.11:g.129377761G>A, NM_002316.3:c.239G>A (LMX1B))

Chromosome 9
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.129377761G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID LMX1B_000165 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-11-27 17:35:39 +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     
LMX1B NM_001174146.1 ?/. - c.239G>A r.(?) p.(Cys80Tyr)
LMX1B NM_001174147.1 ?/. - c.239G>A r.(?) p.(Cys80Tyr)
LMX1B NM_002316.3 ?/. - c.239G>A r.(?) p.(Cys80Tyr)


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