Variant #0000575357 (NC_000023.10:g.24331194T>C, NM_001136233.1:c.239A>G (SUPT20HL2))

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.24331194T>C
DNA change (hg38) g.24313077T>C
Published as SUPT20HL2(NM_001136233.1):c.239A>G (p.(Asn80Ser)), SUPT20HL2(NM_001136233.2):c.317A>G (p.N106S)
ISCN -
DB-ID SUPT20HL2_000014 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) 0.00038 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUPT20HL2 NM_001136233.1 -?/. - c.239A>G r.(?) p.(Asn80Ser)


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