Variant: X:152991228 C / T

: Exomes

Genomes

Total
Filter
Allele Count
Allele Number
Allele Frequency
dbSNP: rs782525046
UCSC: X-152991228-C-T
ClinVar: Click to search for variant in Clinvar

Genotype Quality Metrics

Note: Plot may include low-quality genotypes that were excluded from allele counts in the table above

Site Quality Metrics

Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.

Report this variant

Annotations

This variant falls on 11 transcripts in 2 genes:

synonymous

ABCD1 - ENST00000218104 *

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.

Population Frequencies

Population	Allele Count	Allele Number	Number of Homozygotes	Number of Hemizygotes	Allele Frequency
European (Non-Finnish)
Ashkenazi Jewish*
East Asian
Other
African
Latino
South Asian
European (Finnish)
Total

Include:

Exomes

Genomes

Read Data

This interactive IGV.js visualization shows reads that went into calling this variant.
Note: These are reassembled reads produced by GATK HaplotypeCaller --bamOutput so they accurately represent what HaplotypeCaller was seeing when it called this variant.

Exomes:

Genomes: