Variant #0000563302 (NC_000017.10:g.76568929G>C, NM_173628.3:c.393C>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.76568929G>C
DNA change (hg38) g.78572847G>C
Published as DNAH17(NM_173628.3):c.393C>G (p.P131=)
ISCN -
DB-ID DNAH17_000054
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) 0.00027 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 13:36:11 +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.*148798G>C r.(=) p.(=)
DNAH17 NM_173628.3 -?/. - c.393C>G r.(?) p.(Pro131=)


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