Variant #0000624709 (NC_000023.10:g.71425175C>T, NM_006223.3:c.*7799C>T (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.71425175C>T
DNA change (hg38) g.72205325C>T
Published as ERCC6L(NM_001009954.2):c.3073G>A (p.G1025R), ERCC6L(NM_017669.2):c.3442G>A (p.(Gly1148Arg))
ISCN -
DB-ID ERCC6L_000001 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) 0.00061 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +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     
PIN4 NM_006223.3 -?/. - c.*7799C>T r.(=) p.(=)
ERCC6L NM_017669.2 -?/. - c.3442G>A r.(?) p.(Gly1148Arg)


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