Variant #0000726636 (NC_000017.10:g.66416504T>C, NM_002734.4:c.-92192T>C (PRKAR1A))

Chromosome 17
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.66416504T>C
DNA change (hg38) -
Published as ARSG(NM_014960.4):c.1478T>C (p.I493T)
ISCN -
DB-ID SLC16A6_000009
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) 0.00262 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 ?/. - c.1478T>C r.(?) p.(Ile493Thr)
PRKAR1A NM_002734.4 ?/. - c.-92192T>C r.(?) p.(=)
SLC16A6 NM_004694.4 ?/. - c.-129285A>G r.(?) p.(=)
ARSG NM_014960.3 ?/. - c.1478T>C r.(?) p.(Ile493Thr)
ARSG NM_014960.4 ?/. - c.1478T>C r.(?) p.(Ile493Thr)
WIPI1 NM_017983.5 ?/. - c.*1410A>G r.(=) p.(=)


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