Variant #0000546959 (NC_000012.11:g.124242476_124242477insTTTT, NM_207437.3:c.-4591_-4590insTTTT (DNAH10))

Chromosome 12
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.124242476_124242477insTTTT
DNA change (hg38) g.123757929_123757930insTTTT
Published as ATP6V0A2(NM_012463.3):c.2467_2468insTTTT (p.(Glu824PhefsTer29))
ISCN -
DB-ID ATP6V0A2_000045
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-03 12:59:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP6V0A2 NM_012463.3 -?/. - c.2468_2469insTTTT r.(?) p.(Glu824PhefsTer29)
DNAH10 NM_207437.3 -?/. - c.-4591_-4590insTTTT r.(?) p.(=)


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