Variant #0000281395 (NC_000007.13:g.27135314C>T, NM_005522.4:c.218= (HOXA1))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27135314C>T
DNA change (hg38) g.27095695C>T
Published as HOXA1(NM_005522.5):c.216_218delTCGinsTCA (p.R73H), HOXA1(NM_005522.5):c.218G>A (p.R73H)
ISCN -
DB-ID HOXA1_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) 0.7573 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.218= r.(=) p.(His73=)
HOXA2 NM_006735.3 -/. - c.*5031G>A r.(=) p.(=)


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