Variant #0000571590 (NC_000022.10:g.25023406G>A, NM_013430.2:c.1028G>A (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.25023406G>A
DNA change (hg38) g.24627439G>A
Published as GGT1(NM_001032364.2):c.1028G>A (p.(Arg343His))
ISCN -
DB-ID FAM211B_000002
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) 0.00067 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
GGT1 NM_013430.2 -?/. - c.1028G>A r.(?) p.(Arg343His)
FAM211B NM_207644.2 -?/. - c.-34400C>T r.(?) p.(=)


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