Variant #0000577108 (NC_000023.10:g.69263514T>C, NM_001399.4:c.*8055T>C (EDA))

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.69263514T>C
DNA change (hg38) g.70043664T>C
Published as AWAT2(NM_001002254.1):c.286A>G (p.(Ile96Val))
ISCN -
DB-ID AWAT2_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) 0.00548 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 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     
AWAT2 NM_001002254.1 -?/. - c.286A>G r.(?) p.(Ile96Val)
EDA NM_001399.4 -?/. - c.*8055T>C r.(=) p.(=)


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