Variant #0000543901 (NC_000011.9:g.4112541C>T, NM_001277961.1:c.1889C>T (STIM1))

Chromosome 11
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.4112541C>T
DNA change (hg38) g.4091311C>T
Published as STIM1(NM_001277961.1):c.1889C>T (p.S630F), STIM1(NM_003156.3):c.1571C>T (p.S524F)
ISCN -
DB-ID STIM1_000016 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) 0.00176 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 2024-04-19 20:27:30 +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.-3702C>T r.(?) p.(=)
STIM1 NM_001277961.1 -?/. - c.1889C>T r.(?) p.(Ser630Phe)


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