Variant #0001003364 (NC_000017.10:g.46632808C>G, NC_000017.10(NM_002146.4):c.-159+85G>C (HOXB3))

Chromosome 17
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.46632808C>G
DNA change (hg38) -
Published as HOXB3(NM_002146.4):c.-159+85G>C
ISCN -
DB-ID HOXB2_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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     
HOXB2 NM_002145.3 -?/. - c.-10535G>C r.(?) p.(=)
HOXB3 NM_002146.4 -?/. - c.-159+85G>C r.(=) p.(=)
HOXB4 NM_024015.4 -?/. - c.*21276G>C r.(=) p.(=)


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