Variant #0000608787 (NC_000003.11:g.50229224C>T, NM_144499.2:c.66C>T (GNAT1))

Chromosome 3
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.50229224C>T
DNA change (hg38) g.50191791C>T
Published as GNAT1(NM_144499.3):c.66C>T (p.D22=)
ISCN -
DB-ID SEMA3F_000006
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) 0.0001 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA3F NM_004186.3 -?/. - c.*3676C>T r.(=) p.(=)
GNAT1 NM_144499.2 -?/. - c.66C>T r.(?) p.(Asp22=)


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