Variant #0000275838 (NC_000011.9:g.102991197C>T, NM_001080463.1:c.1021C>T (DYNC2H1))

Chromosome 11
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.102991197C>T
DNA change (hg38) g.103120468C>T
Published as DYNC2H1(NM_001080463.1):c.1021C>T (p.H341Y), DYNC2H1(NM_001080463.2):c.1021C>T (p.H341Y)
ISCN -
DB-ID DYNC2H1_000020 See all 3 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) 0.10365 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     
DYNC2H1 NM_001080463.1 -/. - c.1021C>T r.(?) p.(His341Tyr)


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