Variant #0001003295 (NC_000017.10:g.41738577G>A, NM_004527.3:c.326C>T (MEOX1))

Chromosome 17
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.41738577G>A
DNA change (hg38) -
Published as MEOX1(NM_004527.3):c.326C>T (p.(Pro109Leu))
ISCN -
DB-ID MEOX1_000014
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
MEOX1 NM_001040002.1 -?/. - c.-20C>T r.(?) p.(=)
MEOX1 NM_004527.3 -?/. - c.326C>T r.(?) p.(Pro109Leu)


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