Variant #0001043052 (NC_000019.9:g.46319806G>A, NM_030785.3:c.-1372C>T (RSPH6A))

Chromosome 19
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.46319806G>A
DNA change (hg38) -
Published as SYMPK(NM_004819.3):c.3288C>T (p.(Thr1096=))
ISCN -
DB-ID RSPH6A_000010
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) 0.00254 View details
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     
SYMPK NM_004819.2 -?/. - c.3288C>T r.(?) p.(=)
RSPH6A NM_030785.3 -?/. - c.-1372C>T r.(?) p.(=)


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