Variant #0000526947 (NC_000006.11:g.116938248_116938255del, NM_001010892.2:c.462_469del (RSPH4A))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.116938248_116938255del
DNA change (hg38) g.116617085_116617092del
Published as RSPH4A(NM_001010892.2):c.462_469delGCAACCCA (p.Q155Tfs*12)
ISCN -
DB-ID RSPH4A_000017 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 20:02:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RSPH4A NM_001010892.2 +/. - c.462_469del r.(?) p.(Gln155ThrfsTer12)


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