Variant #0000996589 (NC_000007.13:g.590195C>T, NM_017802.3:c.-176163C>T (HEATR2))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.590195C>T
DNA change (hg38) -
Published as PRKAR1B(NM_001164760.1):c.1018G>A (p.(Val340Met)), PRKAR1B(NM_001164761.2):c.1018G>A (p.V340M)
ISCN -
DB-ID PRKAR1B_000004 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) 0.00031 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKAR1B NM_001164758.1 ?/. - c.1018G>A r.(?) p.(Val340Met)
HEATR2 NM_017802.3 ?/. - c.-176163C>T r.(?) p.(=)


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