Variant #0000690404 (NC_000009.11:g.129376764G>C, NM_002316.3:c.36G>C (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.129376764G>C
DNA change (hg38) -
Published as LMX1B(NM_001174146.1):c.36G>C (p.(Arg12Ser))
ISCN -
DB-ID LMX1B_000204
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.36G>C r.(?) p.(Arg12Ser)
LMX1B NM_001174147.1 -?/. - c.36G>C r.(?) p.(Arg12Ser)
LMX1B NM_002316.3 -?/. - c.36G>C r.(?) p.(Arg12Ser)


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