Variant #0000331746 (NC_000007.13:g.100285473C>T, NM_022574.4:c.199G>A (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.100285473C>T
DNA change (hg38) g.100687850C>T
Published as GIGYF1(NM_001375765.1):c.199G>A (p.A67T), GIGYF1(NM_022574.4):c.199G>A (p.(Ala67Thr))
ISCN -
DB-ID GIGYF1_000003 See all 2 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) 0.00147 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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GIGYF1 NM_022574.4 ?/. - c.199G>A r.(?) p.(Ala67Thr)


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