Version: 8.0.0
Date: Tue Jan 28 2025
9 results
Allele/Variant Genes: HSPA1B (Hsa)

(GRCh38)6:31828417A>G

(Homo sapiens)
Allele/Variant
Source: rs1294280713
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31828417A>G

(GRCh38)6:31829604G>A

(Homo sapiens)
Allele/Variant
Source: rs759701257
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31829604G>A

(GRCh38)6:31829495C>G

(Homo sapiens)
Allele/Variant
Source: rs17854926
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31829495C>G

(GRCh38)6:31829679G>A

(Homo sapiens)
Allele/Variant
Source: rs1267506041
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31829679G>A

(GRCh38)6:31829850G>A

(Homo sapiens)
Allele/Variant
Source: rs558798778
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31829850G>A

(GRCh38)6:31827773C>T

(Homo sapiens)
Allele/Variant
Source: rs6457452
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31827773C>T

(GRCh38)6:31829851G>A

(Homo sapiens)
Allele/Variant
Source: rs1294187054
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31829851G>A

(GRCh38)6:31828143A>G

(Homo sapiens)
Allele/Variant
Source: rs748823567
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31828143A>G

(GRCh38)6:31829836G>A

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.31829836G>A
Genes: SNHG32 (Hsa), HSPA1B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:31829836G>A