Variant #0000984143 (NC_000022.10:g.25007202A>G, NM_013430.2:c.154A>G (GGT1))

Chromosome 22
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.25007202A>G
DNA change (hg38) -
Published as GGT1(NM_001288833.2):c.154A>G (p.(Lys52Glu))
ISCN -
DB-ID FAM211B_000018
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) 0.00238 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GGT1 NM_013430.2 -?/. - c.154A>G r.(?) p.(Lys52Glu)
FAM211B NM_207644.2 -?/. - c.-18196T>C r.(?) p.(=)


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