Variant #0000619121 (NC_000023.10:g.149639348_149639350dup, NM_005491.3:c.1503_1505dup (MAMLD1))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.149639348_149639350dup
DNA change (hg38) g.150471076_150471078dup
Published as MAMLD1(NM_005491.4):c.1503_1505dupGCA (p.Q502dup)
ISCN -
DB-ID MAMLD1_000069
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
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     
MAMLD1 NM_005491.3 -/. - c.1503_1505dup r.(?) p.(Gln502dup)


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