Variant #0000803272 (NC_000007.13:g.88423597G>A, NC_000007.13(NM_181646.2):c.108+34199G>A (ZNF804B))

Chromosome 7
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.88423597G>A
DNA change (hg38) -
Published as TEX47(NM_152706.4):c.660C>T (p.S220=)
ISCN -
DB-ID C7orf62_000004
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) 0.00053 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 2021-09-17 14:40:49 +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     
C7orf62 NM_152706.3 -?/. - c.660C>T r.(?) p.(Ser220=)
ZNF804B NM_181646.2 -?/. - c.108+34199G>A r.(=) p.(=)


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