Variant #0000256147 (NC_000001.10:g.155698848A>C, NM_139118.2:c.-40081T>G (YY1AP1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.155698848A>C
DNA change (hg38) g.155729057A>C
Published as DAP3(NM_001199849.1):c.619A>C (p.K207Q)
ISCN -
DB-ID DAP3_000002
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAP3 NM_004632.3 ?/. - c.619A>C r.(?) p.(Lys207Gln)
YY1AP1 NM_139118.2 ?/. - c.-40081T>G r.(?) p.(=)


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