Variant #0000337941 (NC_000015.9:g.38631920G>A, SPRED1(NM_152594.2):c.424-18G>A)

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38631920G>A
DNA change (hg38) g.38339719G>A
Published as SPRED1(NM_152594.2):c.424-18G>A, SPRED1(NM_152594.3):c.424-18G>A
ISCN -
DB-ID SPRED1_000172 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.22351 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPRED1 NM_152594.2 -/. - c.424-18G>A r.(=) p.(=)