Variant #0000288320 (NC_000007.13:g.100279705T>C, NM_022574.4:c.2915A>G (GIGYF1))

Chromosome 7
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.100279705T>C
DNA change (hg38) g.100682082T>C
Published as GIGYF1(NM_022574.5):c.2915A>G (p.Q972R)
ISCN -
DB-ID GIGYF1_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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
GNB2 NM_005273.3 ?/. - c.*3281T>C r.(=) p.(=)
GIGYF1 NM_022574.4 ?/. - c.2915A>G r.(?) p.(Gln972Arg)


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