Variant #0000964555 (NC_000007.13:g.27182779C>T, NM_002141.4:c.-12427G>A (HOXA4))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.27182779C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HOXA3_000010
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) 0 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +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     
HOXA4 NM_002141.4 ?/. - c.-12427G>A r.(?) p.(=)
HOXA7 NM_006896.3 ?/. - c.*11749G>A r.(=) p.(=)
HOXA5 NM_019102.3 ?/. - c.448G>A r.(?) p.(Glu150Lys)
HOXA6 NM_024014.3 ?/. - c.*2498G>A r.(=) p.(=)
HOXA3 NM_030661.4 ?/. - c.-23765G>A r.(?) p.(=)


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