Variant #0000541827 (NC_000011.9:g.102991668C>A, NM_001080463.1:c.1263C>A (DYNC2H1))

Chromosome 11
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.102991668C>A
DNA change (hg38) g.103120939C>A
Published as DYNC2H1(NM_001080463.1):c.1263C>A (p.F421L), DYNC2H1(NM_001377.2):c.1263C>A (p.(Phe421Leu))
ISCN -
DB-ID DYNC2H1_000023 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) 0.00332 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYNC2H1 NM_001080463.1 -?/. - c.1263C>A r.(?) p.(Phe421Leu)


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