chr1:198719615:A>G Detail (hg19) (PTPRC)

Information

Genome

Assembly Position
hg19 chr1:198,719,615-198,719,615
hg38 chr1:198,750,486-198,750,486 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_002838.4:c.3073-6A>G
NM_080921.3:c.2590-6A>G
Ensemble ENST00000697632.1:c.2035-6A>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Conflicting classifications of pathogenicity
Review star
Show details
Links
Type Database ID Link
Gene MIM 151460 OMIM
HGNC 9666 HGNC
Ensembl ENSG00000081237 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Conflicting interpretations of pathogenicity 2024-01-29 criteria provided, conflicting interpretations Immunodeficiency 104 germline Detail
Likely benign 2022-08-01 criteria provided, single submitter not provided germline Detail
Uncertain significance 2021-03-30 criteria provided, single submitter Immunodeficiency 105 germline Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_002838.5(PTPRC):c.3073-6A>G AND Immunodeficiency 104 ClinVar Detail
NM_002838.5(PTPRC):c.3073-6A>G AND not provided ClinVar Detail
NM_002838.5(PTPRC):c.3073-6A>G AND Immunodeficiency 105 ClinVar Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs191867796 dbSNP
Genome
hg19
Position
chr1:198,719,615-198,719,615
Variant Type
snv
Reference Allele
A
Alternative Allele
G
East Asian Chromosome Counts (ExAC)
8572
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
120934
Allele Counts in All Race (ExAC)
46
Heterozygous Counts in All Race (ExAC)
46
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
3.803727653100038E-4
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