Variant #0000557874 (NC_000016.9:g.30723222G>A, NM_006662.2:c.1559G>A (SRCAP))

Chromosome 16
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.30723222G>A
DNA change (hg38) g.30711901G>A
Published as SRCAP(NM_006662.2):c.1559G>A (p.S520N, p.(Ser520Asn)), SRCAP(NM_006662.3):c.1559G>A (p.S520N)
ISCN -
DB-ID SRCAP_000070 See all 3 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) 0.00122 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRCAP NM_006662.2 -?/. - c.1559G>A r.(?) p.(Ser520Asn)


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