Variant #0000323956 (NC_000015.9:g.30664545C>T, NC_000015.9(NM_148911.1):c.56-1G>A (CHRFAM7A))

Chromosome 15
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.30664545C>T
DNA change (hg38) g.30372342C>T
Published as CHRFAM7A(NM_139320.1):c.329-1G>A (p.?)
ISCN -
DB-ID CHRFAM7A_000001
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 09:36:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHRFAM7A NM_148911.1 ?/. - c.56-1G>A r.spl? p.?


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