Variant #0000517509 (NC_000003.11:g.121518221A>G, NM_001023570.2:c.588T>C (IQCB1))

Chromosome 3
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.121518221A>G
DNA change (hg38) g.121799374A>G
Published as IQCB1(NM_001023570.2):c.588T>C (p.(=)), IQCB1(NM_001023570.3):c.588T>C (p.S196=), IQCB1(NM_001023570.4):c.588T>C (p.S196=)
ISCN -
DB-ID IQCB1_000028 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) 0.00078 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IQCB1 NM_001023570.2 -?/. - c.588T>C r.(?) p.(Ser196=)


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