Variant #0000334637 (NC_000023.10:g.71427424C>T, NM_006223.3:c.*10048C>T (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.71427424C>T
DNA change (hg38) g.72207574C>T
Published as ERCC6L(NM_001009954.2):c.824G>A (p.R275H), ERCC6L(NM_017669.2):c.1193G>A (p.(Arg398His))
ISCN -
DB-ID ERCC6L_000007 See all 2 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) 0.00015 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 2022-05-09 15:51:19 +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.*10048C>T r.(=) p.(=)
ERCC6L NM_017669.2 ?/. - c.1193G>A r.(?) p.(Arg398His)


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