Variant #0000246199 (NC_000003.11:g.57898399A>G, NM_007159.2:c.1889A>G (SLMAP))

Chromosome 3
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.57898399A>G
DNA change (hg38) g.57912672A>G
Published as SLMAP(NM_001304420.3):c.1940A>G (p.Q647R), SLMAP(NM_007159.5):c.1889A>G (p.Q630R)
ISCN -
DB-ID SLMAP_000017 See all 3 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) 0.00052 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLMAP NM_007159.2 ?/. - c.1889A>G r.(?) p.(Gln630Arg)


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