171 results for NGF-AS1

NGF-AS1

(Homo sapiens)
Gene
Name: NGF antisense RNA 1
Synonyms: Not Available
Source: HGNC:53922
Biotype: ncRNA gene
Symbol: NGF-AS1 (Hsa)
Symbol: NGF-AS1

Allele/Variant
Source: rs207460398
Genes: NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115255693G>A

Allele/Variant
Source: rs775686730
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286534G>A

Allele/Variant
Source: rs6325
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286742C>T

Allele/Variant
Source: rs11466110
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286582C>T

Allele/Variant
Source: rs149823633
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286351C>T

Allele/Variant
Source: rs750829893
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286609C>T

Allele/Variant
Source: rs2101018849
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286407C>T

Allele/Variant
Source: rs149876217
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286631C>G

Allele/Variant
Source: NC_000001.11:g.115286458A>G
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286458A>G

Allele/Variant
Source: rs147763877
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286461G>T

Allele/Variant
Source: rs112292538
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286166C>T

Allele/Variant
Source: rs1326012011
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286116G>T

Allele/Variant
Source: rs1553234714
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286124C>T

Allele/Variant
Source: rs1553234715
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286126G>A

Allele/Variant
Source: rs1057524350
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286131A>C

Allele/Variant
Source: rs11466112
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286135G>A

Allele/Variant
Source: rs748481624
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286313T>C

Allele/Variant
Source: rs745359909
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286292A>T

Allele/Variant
Source: rs11466098
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115293399C>T

Allele/Variant
Source: rs771270154
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286513G>T

Allele/Variant
Source: rs774626005
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286196A>G

Allele/Variant
Source: rs572066909
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286594G>A

Allele/Variant
Source: rs746897874
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286397G>T

Allele/Variant
Source: rs1258866875
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286672G>A

Allele/Variant
Source: rs1258866875
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286672G>C

Allele/Variant
Source: rs267597943
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286690G>T

Allele/Variant
Source: rs139541754
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286288A>G

Allele/Variant
Source: rs1653498654
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286305T>A

Allele/Variant
Source: rs3738701
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115293482G>T

Allele/Variant
Source: rs550213301
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115338191C>A

Allele/Variant
Source: rs985498627
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286158A>G

Allele/Variant
Source: rs1571069537
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286328C>T

Allele/Variant
Source: rs147763877
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286461G>C

Allele/Variant
Source: rs2101019050
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286521T>C

Allele/Variant
Source: rs767272925
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286548C>T

Allele/Variant
Source: rs138175552
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286549G>A

Allele/Variant
Source: rs766912679
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286642G>A

Allele/Variant
Source: rs1294782064
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286660T>C

Allele/Variant
Source: rs769465872
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286713G>T

Allele/Variant
Source: rs149823633
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286351C>A

Allele/Variant
Source: NC_000001.11:g.115286252G>A
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286252G>A

Allele/Variant
Source: rs780383333
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286577G>A

Allele/Variant
Source: rs755243469
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286612G>T

Allele/Variant
Source: rs149876217
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286631C>T

Allele/Variant
Source: rs2101018914
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286442C>T

Allele/Variant
Source: rs200459956
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286636C>T

Allele/Variant
Source: NC_000001.11:g.115286701A>G
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286701A>G

Allele/Variant
Source: rs11466111
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286557C>T

Allele/Variant
Source: NC_000001.11:g.115286555G>A
Genes: NGF (Hsa), NGF-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:115286555G>A