Variant #0001056199 (NC_000017.10:g.76488805T>G, NM_173628.3:c.6451A>C (DNAH17))

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.76488805T>G
DNA change (hg38) -
Published as DNAH17(NM_173628.4):c.6451A>C (p.(Lys2151Gln))
ISCN -
DB-ID DNAH17_000119
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
PGS1 NM_024419.3 -?/. - c.*68674T>G r.(=) p.(=)
DNAH17 NM_173628.3 -?/. - c.6451A>C r.(?) p.(Lys2151Gln)
DNAH17-AS1 NR_102401.1 -?/. - n.454-364T>G r.(?) -


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