Variant #0000331492 (NC_000007.13:g.27135273C>T, NM_005522.4:c.259G>A (HOXA1))

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.27135273C>T
DNA change (hg38) g.27095654C>T
Published as HOXA1(NM_005522.4):c.259G>A (p.(Gly87Arg))
ISCN -
DB-ID HOXA1_000001
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) 2.0E-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 2018-01-15 20:58:59 +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     
HOXA1 NM_005522.4 ?/. - c.259G>A r.(?) p.(Gly87Arg)
HOXA2 NM_006735.3 ?/. - c.*5072G>A r.(=) p.(=)


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