Variant #0000808782 (NC_000019.9:g.1912297C>G, NM_138422.2:c.251C>G (ADAT3))

Chromosome 19
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.1912297C>G
DNA change (hg38) -
Published as ADAT3(NM_138422.4):c.251C>G (p.P84R)
ISCN -
DB-ID ADAT3_000006
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) 0.00012 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCAMP4 NM_079834.2 ?/. - c.-41-2681C>G r.(=) p.(=)
ADAT3 NM_138422.2 ?/. - c.251C>G r.(?) p.(Pro84Arg)


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