Variant #0000611854 (NC_000009.11:g.129377769T>C, NM_002316.3:c.247T>C (LMX1B))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.129377769T>C
DNA change (hg38) g.126615490T>C
Published as LMX1B(NM_001174146.2):c.247T>C (p.C83R)
ISCN -
DB-ID LMX1B_000017 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LMX1B NM_001174146.1 +/. - c.247T>C r.(?) p.(Cys83Arg)
LMX1B NM_001174147.1 +/. - c.247T>C r.(?) p.(Cys83Arg)
LMX1B NM_002316.3 +/. - c.247T>C r.(?) p.(Cys83Arg)


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