Variant #0000567276 (NC_000019.9:g.3910894C>T, ATCAY(NM_033064.4):c.866+7C>T)

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.3910894C>T
DNA change (hg38) g.3910896C>T
Published as ATCAY(NM_033064.4):c.866+7C>T (, p.(=))
ISCN -
DB-ID ATCAY_000016 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) 0.00169 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATCAY NM_033064.4 -?/. - c.866+7C>T r.(=) p.(=)