Variant #0000894358 (NC_000017.10:g.79892230C>T, NM_006907.2:c.769G>A (PYCR1))

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.79892230C>T
DNA change (hg38) -
Published as PYCR1(NM_006907.2):c.769G>A (p.(Ala257Thr)), PYCR1(NM_006907.3):c.769G>A (p.A257T)
ISCN -
DB-ID PYCR1_000007 See all 4 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) 3.0E-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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PYCR1 NM_006907.2 ?/. - c.769G>A r.(?) p.(Ala257Thr)


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