Variant #0000270145 (NC_000008.10:g.61654298T>A, NM_017780.3:c.307T>A (CHD7))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61654298T>A
DNA change (hg38) g.60741739T>A
Published as CHD7(NM_017780.2):c.307T>A (p.S103T), CHD7(NM_017780.3):c.307T>A (p.(Ser103Thr)), CHD7(NM_017780.4):c.307T>A (p.S103T)
ISCN -
DB-ID CHD7_000011 See all 4 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) 0.01228 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
CHD7 NM_017780.3 -/. - c.307T>A r.(?) p.(Ser103Thr)


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