Variant #0000257858 (NC_000010.10:g.92678744_92678761del, NC_000010.10(NM_014391.2):c.346-29_346-12del (ANKRD1))

Chromosome 10
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.92678744_92678761del
DNA change (hg38) g.90918987_90919004del
Published as ANKRD1(NM_014391.2):c.346-35_346-12delATATATATATATATATTTATTTATinsATATAT, ANKRD1(NM_014391.2):c.346-35_346-15delATATATATATATATATTTATTinsATA, ANKRD1...
ISCN -
DB-ID ANKRD1_000031 See all 6 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) 0.56127 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD1 NM_014391.2 -/. - c.346-29_346-12del r.(=) p.(=)


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