Variant #0000326264 (NC_000019.9:g.14200871_14200876del, NM_002730.3:c.*3056_*3061del (PRKACA))

Chromosome 19
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.14200871_14200876del
DNA change (hg38) g.14090059_14090064del
Published as SAMD1(NM_138352.1):c.336+29_336+34del (p.(Pro122_Pro123del))
ISCN -
DB-ID SAMD1_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKACA NM_002730.3 ?/. - c.*3056_*3061del r.(=) p.(=)
SAMD1 NM_138352.1 ?/. - c.365_370del r.(?) p.(Pro122_Pro123del)


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