Variant #0000538987 (NC_000010.10:g.104629554C>G, NC_000010.10(NM_020682.3):c.2-8C>G (AS3MT))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.104629554C>G
DNA change (hg38) g.102869797C>G
Published as AS3MT(NM_020682.3):c.2-8C>G (p.(=))
ISCN -
DB-ID AS3MT_000001
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) 0.00013 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AS3MT NM_020682.3 ?/. - c.2-8C>G r.(=) p.(=)
C10orf32 NM_144591.3 ?/. - c.*6076C>G r.(=) p.(=)


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