Variant #0000865969 (NC_000019.9:g.18895853G>T, NM_000095.2:c.1767C>A (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.18895853G>T
DNA change (hg38) -
Published as COMP(NM_000095.2):c.1767C>A (p.(Asn589Lys))
ISCN -
DB-ID COMP_000178
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COMP NM_000095.2 ?/. - c.1767C>A r.(?) p.(Asn589Lys)
CRTC1 NM_001098482.1 ?/. - c.*7661G>T r.(=) p.(=)


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