Variant #0000656689 (NC_000011.9:g.117252598_117252621del, NC_000011.9(NM_014956.4):c.1577+14_1577+37del (CEP164))

Chromosome 11
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.117252598_117252621del
DNA change (hg38) g.117381882_117381905del
Published as CEP164(NM_014956.4):c.1577+14_1577+37delGAAGCATCCTCATGAGGATGAGGG
ISCN -
DB-ID CEP164_000083
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP164 NM_014956.4 -?/. - c.1577+14_1577+37del r.(=) p.(=)


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