Variant #0001040904 (NC_000016.9:g.21136599_21136600del, NM_017539.1:c.1300_1301del (DNAH3))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21136599_21136600del
DNA change (hg38) -
Published as DNAH3(NM_001347886.2):c.1213_1214del (p.(Ile405*))
ISCN -
DB-ID DNAH3_000050
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAH3 NM_017539.1 ?/. - c.1300_1301del r.(?) p.(Ile434*)
TMEM159 NM_020422.4 ?/. - c.-33674_-33673del r.(?) p.(=)


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