Variant #0000611206 (NC_000007.13:g.781069_781070insGG, NM_017802.3:c.991_992insGG (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.781069_781070insGG
DNA change (hg38) g.741432_741433insGG
Published as HEATR2(NM_017802.3):c.990_991insGG (p.(Ala331GlyfsTer48))
ISCN -
DB-ID HEATR2_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-22 13:21:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKAR1B NM_001164758.1 -?/. - c.-13865_-13864insCC r.(?) p.(=)
HEATR2 NM_017802.3 -?/. - c.991_992insGG r.(?) p.(Ala331GlyfsTer48)


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