Variant #0000532427 (NC_000007.13:g.635849G>A, NM_017802.3:c.-130509G>A (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.635849G>A
DNA change (hg38) g.596212G>A
Published as PRKAR1B(NM_001164761.1):c.642C>T (p.T214=), PRKAR1B(NM_001164761.2):c.642C>T (p.T214=)
ISCN -
DB-ID PRKAR1B_000014 See all 2 reported entries
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) 0.00161 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.642C>T r.(?) p.(Thr214=)
HEATR2 NM_017802.3 -?/. - c.-130509G>A r.(?) p.(=)


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