Variant #0000521514 (NC_000004.11:g.123848876G>A, NM_145207.2:c.251G>A (SPATA5))

Chromosome 4
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.123848876G>A
DNA change (hg38) g.122927721G>A
Published as SPATA5(NM_001317799.1):c.248G>A (p.(Arg83Gln)), SPATA5(NM_145207.2):c.251G>A (p.R84Q)
ISCN -
DB-ID SPATA5_000006 See all 5 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) 7.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGF2 NM_002006.4 ?/. - c.*35325G>A r.(=) p.(=)
NUDT6 NM_007083.4 ?/. - c.-5149C>T r.(?) p.(=)
SPATA5 NM_145207.2 ?/. - c.251G>A r.(?) p.(Arg84Gln)


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