Variant #0000334635 (NC_000023.10:g.71427042T>C, NM_006223.3:c.*9666T>C (PIN4))

Chromosome X
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.71427042T>C
DNA change (hg38) g.72207192T>C
Published as ERCC6L(NM_017669.2):c.1575A>G (p.(=))
ISCN -
DB-ID ERCC6L_000005
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) 0.0026 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-20 15:10:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIN4 NM_006223.3 ?/. - c.*9666T>C r.(=) p.(=)
ERCC6L NM_017669.2 ?/. - c.1575A>G r.(?) p.(Gln525=)


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