Variant #0000611033 (NC_000007.13:g.27224432G>A, NM_018951.3:c.-10507C>T (HOXA10))

Chromosome 7
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.27224432G>A
DNA change (hg38) g.27184813G>A
Published as HOXA11(NM_005523.5):c.332C>T (p.(Ser111Leu))
ISCN -
DB-ID HOXA9_000003
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXA11 NM_005523.5 -?/. - c.332C>T r.(?) p.(Ser111Leu)
HOXA10 NM_018951.3 -?/. - c.-10507C>T r.(?) p.(=)
HOXA9 NM_152739.3 -?/. - c.-19356C>T r.(?) p.(=)


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