Variant #0000577348 (NC_000023.10:g.71426078T>C, NM_006223.3:c.*8702T>C (PIN4))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71426078T>C
DNA change (hg38) g.72206228T>C
Published as ERCC6L(NM_017669.4):c.2539A>G (p.T847A)
ISCN -
DB-ID PIN4_000011
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
PIN4 NM_006223.3 -?/. - c.*8702T>C r.(=) p.(=)
ERCC6L NM_017669.2 -?/. - c.2539A>G r.(?) p.(Thr847Ala)


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