Variant #0000989937 (NC_000010.10:g.92679979G>C, NM_014391.2:c.154C>G (ANKRD1))

Chromosome 10
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.92679979G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ANKRD1_000011 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397517248
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-20 17:26:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD1 NM_014391.2 -?/. - c.154C>G r.(?) p.(Pro52Ala)


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