Variant #0000515040 (NC_000002.11:g.232209768G>A, NM_025139.4:c.1960G>A (ARMC9))

Chromosome 2
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.232209768G>A
DNA change (hg38) g.231345056G>A
Published as ARMC9(NM_001271466.1):c.1960G>A (p.(Val654Ile))
ISCN -
DB-ID ARMC9_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARMC9 NM_001352754.1 -?/. - c.1960G>A r.(?) p.(Val654Ile)
ARMC9 NM_025139.4 -?/. - c.1960G>A r.(?) p.(Val654Ile)


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