Variant #0000333165 (NC_000023.10:g.11783771G>A, NM_078629.3:c.1094G>A (MSL3))

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.11783771G>A
DNA change (hg38) g.11765652G>A
Published as MSL3(NM_001193270.1):c.1058G>A (p.(Ser353Asn)), MSL3(NM_001282174.1):c.647G>A (p.S216N)
ISCN -
DB-ID MSL3_000018 See all 3 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) 0.00148 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSL3 NM_078629.3 -?/. - c.1094G>A r.(?) p.(Ser365Asn)


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