Variant #0000325664 (NC_000017.10:g.76449418_76449420del, NC_000017.10(NM_173628.3):c.10529+8_10529+10del (DNAH17))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76449418_76449420del
DNA change (hg38) g.78453336_78453338del
Published as DNAH17(NM_173628.3):c.10529+8_10529+10del (p.(=)), DNAH17(NM_173628.3):c.10529+8_10529+10delGTT
ISCN -
DB-ID DNAH17_000015 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGS1 NM_024419.3 ?/. - c.*29287_*29289del r.(=) p.(=)
DNAH17 NM_173628.3 ?/. - c.10529+8_10529+10del r.(=) p.(=)


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