Variant #0000559341 (NC_000016.9:g.83932955C>T, NM_012213.2:c.206C>T (MLYCD))

Chromosome 16
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.83932955C>T
DNA change (hg38) g.83899350C>T
Published as MLYCD(NM_012213.2):c.206C>T (p.(Ala69Val)), MLYCD(NM_012213.3):c.206C>T (p.A69V)
ISCN -
DB-ID MLYCD_000003 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) 0.00374 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
MLYCD NM_012213.2 -?/. - c.206C>T r.(?) p.(Ala69Val)


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