Variant #0000566639 (NC_000019.9:g.18894001A>G, NM_000095.2:c.2090T>C (COMP))

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.18894001A>G
DNA change (hg38) g.18783191A>G
Published as COMP(NM_000095.2):c.2090T>C (p.(Val697Ala))
ISCN -
DB-ID COMP_000140
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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
COMP NM_000095.2 ?/. - c.2090T>C r.(?) p.(Val697Ala)
CRTC1 NM_001098482.1 ?/. - c.*5809A>G r.(=) p.(=)


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