Variant #0000678876 (NC_000010.10:g.69991427G>A, NM_145178.3:c.8C>T (ATOH7))

Chromosome 10
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.69991427G>A
DNA change (hg38) -
Published as ATOH7(NM_145178.3):c.8C>T (p.S3F), ATOH7(NM_145178.4):c.8C>T (p.(Ser3Phe))
ISCN -
DB-ID ATOH7_000012 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATOH7 NM_145178.3 ?/. - c.8C>T r.(?) p.(Ser3Phe)


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