Variant #0000322627 (NC_000012.11:g.2927299G>A, NM_018463.3:c.262G>A (ITFG2))

Chromosome 12
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.2927299G>A
DNA change (hg38) g.2818133G>A
Published as ITFG2(NM_018463.3):c.262G>A (p.(Gly88Ser))
ISCN -
DB-ID ITFG2_000001
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) Retrieve
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITFG2 NM_018463.3 ?/. - c.262G>A r.(?) p.(Gly88Ser)
NRIP2 NM_031474.2 ?/. - c.*9074C>T r.(=) p.(=)


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