Variant #0000975219 (NC_000002.11:g.29296598G>A, NM_001029883.2:c.530C>T (C2orf71))

Chromosome 2
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.29296598G>A
DNA change (hg38) -
Published as PCARE(NM_001029883.2):c.530C>T (p.P177L), PCARE(NM_001029883.3):c.530C>T (p.(Pro177Leu))
ISCN -
DB-ID C2orf71_000130 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) 0.00033 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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2orf71 NM_001029883.2 ?/. - c.530C>T r.(?) p.(Pro177Leu)


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