Genomic variant #0000005279

Chromosome X
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.153640317C>T
Published as -
GERP -
Segregation -
DB-ID TAZ_000172
dbSNP ID -
Frequency -
Sources ; BSF_TAZ;
Reference -
Variant remarks -
Genetic origin -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

Location     

Exon     

Protein     

GVS function     

Position     

PolyPhen     

RNA change     

Splice distance     

SIFT     
TAZ NM_000116.3 ./. c.109+28C>T - - p.(=) - - - r.(=) - -
DNASE1L1 NM_001009934.1 ./. c.-177G>A - - p.(=) - - - r.(=) - -
TAZ NM_181311.2 ./. c.109+28C>T - - p.(=) - - - r.(=) - -
TAZ NM_181312.2 ./. c.109+28C>T - - p.(=) - - - r.(=) - -
TAZ NM_181313.2 ./. c.109+28C>T - - p.(=) - - - r.(=) - -
TAZ NR_024048.1 ./. n.413+28C>T - - - - - - - - -


ClinVar @ MSeqDR

0.00014
51422
MedGen:CN169374
not specified
HGVS variant names NC 000023.10:g.153640317C>T
criteria provided, single submitter
Clinical Significance
single nucleotide variant
SO:0001483
Gene symbol:Gene id. DNASE1L1:1774|TAZ:6901
SO:0001583|missense variant,SO:0001627|intron variant
1
dbSNP ID 397515736
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None