MAP4K1-AS1

MAP4K1 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 19:38596290-38601705

Links

ENSG00000267291NCBI:105372397HGNC:55302GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the MAP4K1-AS1 gene.

  • Inborn genetic diseases (7 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MAP4K1-AS1 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type Pathogenic Likely pathogenic VUS Likely benign Benign Sum
synonymous
0
missense
0
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
7
clinvar
7
Total 0 0 7 0 0

Variants in MAP4K1-AS1

This is a list of pathogenic ClinVar variants found in the MAP4K1-AS1 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position Type Phenotype Significance ClinVar
19-38596318-T-G not specified Uncertain significance (Nov 06, 2023)3123071
19-38596425-G-C not specified Uncertain significance (Feb 15, 2023)2463727
19-38596446-G-C not specified Uncertain significance (Mar 16, 2022)2278849
19-38597090-T-C not specified Uncertain significance (Dec 01, 2022)2410558
19-38597337-G-A not specified Uncertain significance (Dec 07, 2021)2397055
19-38597522-G-A not specified Uncertain significance (Jan 02, 2024)3123069
19-38600087-G-A not specified Uncertain significance (May 05, 2023)2512846
19-38600149-C-A not specified Uncertain significance (Apr 07, 2023)2534128
19-38601483-G-A not specified Uncertain significance (Jul 17, 2023)2601980

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP