Variant #0000253635 (NC_000017.10:g.76568881A>G, NM_173628.3:c.441T>C (DNAH17))

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.76568881A>G
DNA change (hg38) g.78572799A>G
Published as DNAH17(NM_173628.3):c.441T>C (p.N147=)
ISCN -
DB-ID DNAH17_000030
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) 0.00887 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 13:36:05 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PGS1 NM_024419.3 -/. - c.*148750A>G r.(=) p.(=)
DNAH17 NM_173628.3 -/. - c.441T>C r.(?) p.(Asn147=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.