Variant #0000330429 (NC_000005.9:g.75906923C>G, NM_006633.2:c.1436C>G (IQGAP2))

Chromosome 5
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.75906923C>G
DNA change (hg38) g.76611098C>G
Published as IQGAP2(NM_006633.2):c.1436C>G (p.(Pro479Arg))
ISCN -
DB-ID IQGAP2_000004
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) 0.01229 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F2RL2 NM_001256566.1 ?/. - c.*6484G>C r.(=) p.(=)
IQGAP2 NM_006633.2 ?/. - c.1436C>G r.(?) p.(Pro479Arg)


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