Variant #0000677072 (NC_000003.11:g.57323133G>A, NM_178504.4:c.*4676C>T (DNAH12))

Chromosome 3
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.57323133G>A
DNA change (hg38) -
Published as ASB14(NM_001142733.2):c.141C>T (p.S47=)
ISCN -
DB-ID APPL1_000003
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) 0.00016 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASB14 NM_001142733.2 -?/. - c.141C>T r.(?) p.(Ser47=)
APPL1 NM_012096.2 -?/. - c.*19418G>A r.(=) p.(=)
DNAH12 NM_178504.4 -?/. - c.*4676C>T r.(=) p.(=)


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