Variant #0000993933 (NC_000003.11:g.9074342A>G, NC_000003.11(NM_001033117.2):c.1437-4528T>C (SRGAP3))

Chromosome 3
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.9074342A>G
DNA change (hg38) -
Published as SRGAP3(NM_014850.3):c.1531T>C (p.(Phe511Leu)), SRGAP3(NM_014850.4):c.1531T>C (p.F511L)
ISCN -
DB-ID SRGAP3_000004 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) 0.00262 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 2024-08-28 13:16:32 +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     
SRGAP3 NM_001033117.2 -?/. - c.1437-4528T>C r.(=) p.(=)


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