Variant #0000613335 (NC_000011.9:g.4112773C>G, NM_001277961.1:c.2121C>G (STIM1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4112773C>G
DNA change (hg38) g.4091543C>G
Published as STIM1(NM_001277961.1):c.2121C>G (p.(Pro707=))
ISCN -
DB-ID RRM1_000002
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) 0.00962 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRM1 NM_001033.3 -/. - c.-3470C>G r.(?) p.(=)
STIM1 NM_001277961.1 -/. - c.2121C>G r.(?) p.(Pro707=)


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