View genomic variant #0000000022

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.33502429T>C
Published as -
GERP 4.920
Segregation -
DB-ID AK2_000006 See all 2 reported entries
MSCV MSCV_0000022
dbSNP ID rs137853206
Frequency -
Sources ; clinVar; Ensembl;
Reference 19043417
Variant remarks -
Genetic origin -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
AK2 00000423 NM_001199199.1 0000000022 +/+ - 1/6 c.1A>G p.? - initiator_codon_variant - -
AK2 00000426 NM_001625.3 0000000022 +/+ - 1/6 c.1A>G p.? - initiator_codon_variant - -
AK2 00000424 NM_013411.4 0000000022 +/+ - 1/6 c.1A>G p.? - initiator_codon_variant - -
AK2 00000425 NR_037591.1 0000000022 +/+ - 1/7 n.84A>G - - non_coding_transcript_exon_variant,non_coding_transcript_variant - -
AK2 00000427 NR_037592.1 0000000022 +/+ - 1/7 n.84A>G - - non_coding_transcript_exon_variant,non_coding_transcript_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000019914;
Chromosome 1:33502429..33502429
ClinVar Allele ID 33291
Disease database name and identifier MedGen:C0272167, OMIM:267500, Orphanet:ORPHA33355, SNOMED CT:111584000
ClinVar preferred disease name Reticular dysgenesis
HGVS variant names NC 000001.10:g.33502429T>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported OMIM Allelic Variant:103020.0003
Gene symbol:Gene id. AK2:204
Molecular consequence SO:0001583|missense variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 137853206
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

variation_namechromseq_region_startseq_region_endallele_stringminor_alleleminor_allele_freqvariation_setPhenotype_description
rs13785320613350242933502429T/COMIM phenotype variantsRETICULAR DYSGENESIS
CM09001213350242933502429HGMD_MUTATIONHGMD-PUBLIC variantsAnnotated by HGMD but no phenotype description is publicly available