Variant #0000689986 (NC_000007.13:g.27224296G>C, NM_018951.3:c.-10371C>G (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.27224296G>C
DNA change (hg38) -
Published as HOXA11(NM_005523.5):c.468C>G (p.(=))
ISCN -
DB-ID HOXA9_000006
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) 7.0E-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 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     
HOXA11 NM_005523.5 -?/. - c.468C>G r.(?) p.(Ser156=)
HOXA10 NM_018951.3 -?/. - c.-10371C>G r.(?) p.(=)
HOXA9 NM_152739.3 -?/. - c.-19220C>G r.(?) p.(=)


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