Variant #0000893993 (NC_000017.10:g.46628560G>C, NC_000017.10(NM_002146.4):c.449-17C>G (HOXB3))

Chromosome 17
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.46628560G>C
DNA change (hg38) -
Published as HOXB3(NM_002146.4):c.449-17C>G
ISCN -
DB-ID HOXB2_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) 0.00146 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +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     
HOXB2 NM_002145.3 -/. - c.-6287C>G r.(?) p.(=)
HOXB3 NM_002146.4 -/. - c.449-17C>G r.(=) p.(=)
HOXB4 NM_024015.4 -/. - c.*25524C>G r.(=) p.(=)


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