Variant #0000888617 (NC_000009.11:g.129376788C>T, NM_002316.3:c.60C>T (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.129376788C>T
DNA change (hg38) -
Published as LMX1B(NM_002316.4):c.60C>T (p.D20=)
ISCN -
DB-ID LMX1B_000209
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) 1.0E-5 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 2022-11-01 13:01:21 +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.60C>T r.(?) p.(Asp20=)
LMX1B NM_001174147.1 -?/. - c.60C>T r.(?) p.(Asp20=)
LMX1B NM_002316.3 -?/. - c.60C>T r.(?) p.(Asp20=)


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