Variant #0000566648 (NC_000019.9:g.18897440T>C, NM_000095.2:c.1156A>G (COMP))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18897440T>C
DNA change (hg38) g.18786630T>C
Published as COMP(NM_000095.2):c.1156A>G (p.(Asn386Asp))
ISCN -
DB-ID COMP_000147 See all 3 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) 0.03299 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.1156A>G r.(?) p.(Asn386Asp)
CRTC1 NM_001098482.1 -/. - c.*9248T>C r.(=) p.(=)


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