Variant #0000616860 (NC_000017.10:g.76435298T>C, NM_173628.3:c.11679A>G (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.76435298T>C
DNA change (hg38) g.78439216T>C
Published as DNAH17(NM_173628.3):c.11679A>G (p.G3893=, p.(Gly3893=))
ISCN -
DB-ID DNAH17_000059 See all 2 reported entries
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) 0.00099 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGS1 NM_024419.3 -?/. - c.*15167T>C r.(=) p.(=)
DNAH17 NM_173628.3 -?/. - c.11679A>G r.(?) p.(Gly3893=)


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