Variant #0000299475 (NC_000009.11:g.34637690T>G, NM_005866.2:c.5A>C (SIGMAR1))

Chromosome 9
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.34637690T>G
DNA change (hg38) g.34637693T>G
Published as SIGMAR1(NM_001282208.2):c.5A>C (p.Q2P), SIGMAR1(NM_005866.3):c.5A>C (p.Q2P)
ISCN -
DB-ID SIGMAR1_000010 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) 0.20207 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIGMAR1 NM_005866.2 -/. - c.5A>C r.(?) p.(Gln2Pro)


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