Variant #0000260510 (NC_000014.8:g.69341658G>A, NM_001102.3:c.2597C>T (ACTN1))

Chromosome 14
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.69341658G>A
DNA change (hg38) g.68874941G>A
Published as ACTN1(NM_001102.3):c.2597C>T (p.(Pro866Leu)), ACTN1(NM_001130004.1):c.2663C>T (p.P888L)
ISCN -
DB-ID ACTN1_000008 See all 2 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) 0.02052 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTN1 NM_001102.3 -/. - c.2597C>T r.(?) p.(Pro866Leu)


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