Variant #0000654075 (NC_000001.10:g.57341803G>A, NM_000562.2:c.385G>A (C8A))

Chromosome 1
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.57341803G>A
DNA change (hg38) g.56876130G>A
Published as C8A(NM_000562.2):c.385G>A (p.D129N), C8A(NM_000562.3):c.385G>A (p.D129N)
ISCN -
DB-ID C8A_000009 See all 4 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) 0.00232 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C8A NM_000562.2 -?/. - c.385G>A r.(?) p.(Asp129Asn)


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