Variant #0000250293 (NC_000007.13:g.590124A>G, NM_017802.3:c.-176234A>G (HEATR2))

Chromosome 7
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.590124A>G
DNA change (hg38) g.550487A>G
Published as PRKAR1B(NM_001164761.2):c.1089T>C (p.S363=)
ISCN -
DB-ID PRKAR1B_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) 3.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +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     
PRKAR1B NM_001164758.1 -?/. - c.1089T>C r.(?) p.(Ser363=)
HEATR2 NM_017802.3 -?/. - c.-176234A>G r.(?) p.(=)


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