View genomic variant #0000015105

Chromosome M
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) m.14430A>G
Published as -
GERP -
Segregation -
DB-ID chrM_001134 See all 2 reported entries
MSCV MSCV_0004037
dbSNP ID -
Frequency -
Sources ; Somatic:ICGC;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lishuang Shen




Variant on transcripts

0 entries on 0 pages.
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MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND6Thyroid CancerA14430GW-R+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None