Variant #0000253257 (NC_000007.13:g.21924014A>G, NM_001277115.1:c.12493A>G (DNAH11))

Chromosome 7
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.21924014A>G
DNA change (hg38) g.21884396A>G
Published as DNAH11(NM_001277115.1):c.12493A>G (p.M4165V), DNAH11(NM_001277115.2):c.12493A>G (p.M4165V)
ISCN -
DB-ID DNAH11_000122 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) 0.757 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH11 NM_001277115.1 -/. - c.12493A>G r.(?) p.(Met4165Val)
CDCA7L NM_018719.4 -/. - c.*17926T>C r.(=) p.(=)


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