132593092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28796202-A-T

132593219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28796086-T-C

132593278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28796058-G-T

132593654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795764-T-C

132593824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795665-A-G

http://identifiers.org/hco/9/GRCh38#132593847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28795650-C-A

132593847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795650-C-T

132593868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795629-G-C

132593868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795629-G-T

132593895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795618-G-A

http://identifiers.org/hco/9/GRCh38#132593928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28795586-C-A

132593928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795586-C-T

http://identifiers.org/hco/9/GRCh38#132593992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28795523-A-C

132594047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795499-G-A

132594048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795498-G-A

132594048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795498-G-C

132594048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795498-G-T

132594077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795471-G-T

132594203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795377-G-T

132594395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795200-T-C

http://identifiers.org/hco/9/GRCh38#132594444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28795149-C-A

132594444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795149-C-T

132594452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795141-T-C

http://identifiers.org/hco/9/GRCh38#132594510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28795099-C-A

132594518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795098-T-C

132594518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795098-T-G

132594532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795084-G-A

132594532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28795084-G-T

132594749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28794947-G-T

132594815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28794881-A-G

http://identifiers.org/hco/9/GRCh38#132594892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28794800-C-A

132594892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28794800-C-T

132594901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28794791-C-T

132594912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28794781-G-C

132594912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28794781-G-T

http://identifiers.org/hco/9/GRCh38#132595024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28794693-C-A

132595024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28794693-C-T

132595077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28794634-C-T

132595115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28794596-G-A

132595744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28794054-A-G

132596145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28793742-G-C

132596285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28793624-C-T

132597201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28793350-G-A

132597833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28792849-G-A

132597894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28792791-C-T

132598598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28792200-A-T

132598613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28792187-T-G

132598620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28792180-G-C

132599610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28791455-T-C

132599973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28791181-A-T

132600739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28790282-G-C

http://identifiers.org/hco/9/GRCh38#132601101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28789993-C-A

132601101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789993-C-T

132601113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789981-C-T

http://identifiers.org/hco/9/GRCh38#132601419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28789722-A-C

132601446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789698-T-C

132601484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789662-G-A

132601627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789570-A-G

132602048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789443-G-C

132602081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28789414-T-C

132603347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28788186-C-T

132603507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28788061-G-A

132603507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28788061-G-T

132603827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28787755-T-G

http://identifiers.org/hco/9/GRCh38#132604030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28787550-C-A

132604277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28787391-G-A

132604550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28787265-T-A

132604550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28787265-T-C

132604582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28787226-T-A

132605051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28786851-A-G

132606073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28786280-G-A

132606475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785903-C-T

132606534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785841-T-C

132606596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785782-C-T

132607061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785420-G-A

132607196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785301-C-T

132607208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785289-T-C

132607425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785131-C-G

132607564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28785049-G-A

132608459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28784449-G-A

132608491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28784417-G-A

132608624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28784325-T-C

132608748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28784228-C-T

http://identifiers.org/hco/9/GRCh38#132610865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28783535-A-C

132610869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783531-A-T

132610897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783501-A-G

132611051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783398-G-C

132611153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783327-G-C

132611153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783327-G-T

132611156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783324-C-T

132611164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783315-G-A

132611269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783216-T-C

132611469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28783003-C-T

132612187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28782457-A-T

132612355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28782300-G-A

132612355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28782300-G-T

132612377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28782280-A-G

132614782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28780648-G-T

132614920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28780520-T-C

132615020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28780462-G-A

132615373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28780148-C-T

132615627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28779929-G-A

132615757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28779804-C-T

132615792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28779769-G-A

132616016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28779548-G-C

132616541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28779067-T-C

132617164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28778485-T-A

132617253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28778385-C-T

132617789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28777535-C-T

132618968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28776172-A-G

132618996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28776139-T-C

132619177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28776000-T-A

http://identifiers.org/hco/9/GRCh38#132619394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28775828-C-A

132619564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28775709-G-A

132619658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28775614-G-A

http://identifiers.org/hco/9/GRCh38#132620786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28774550-A-C

132620973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28774367-T-G

132621315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28774033-T-C

132621562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28773787-G-A

132621960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28773476-T-A

http://identifiers.org/hco/9/GRCh38#132622088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28773351-A-C

132622534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28772961-C-T

132624841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771995-G-A

http://identifiers.org/hco/9/GRCh38#132625291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28771585-A-C

132625524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771333-T-C

132625540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771317-T-A

132625540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771317-T-C

132625790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771107-A-G

132625806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771091-G-T

132625832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771065-G-C

132625832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28771065-G-T

132626698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28769760-G-C

132626715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28769743-C-T

132627496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28768964-G-A

132627623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28768873-A-T

132627655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28768854-C-T

132628984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28767317-T-C

132629022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28767280-C-G

132629288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28767022-G-C

132629854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28766222-G-A

132630097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28766005-G-C

132630428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765675-G-A

http://identifiers.org/hco/9/GRCh38#132630429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28765674-C-A

132630449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765654-G-A

132630449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765654-G-T

132630469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765634-T-C

132630515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765611-T-G

132630516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765610-A-G

http://identifiers.org/hco/9/GRCh38#132631078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28765217-C-A

132631078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765217-C-G

132631158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28765148-C-G

132631541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764704-A-T

132631597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764606-T-C

132631614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764589-G-A

132631711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764490-T-C

132631835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764370-A-G

132631865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764339-G-A

http://identifiers.org/hco/9/GRCh38#132631989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28764230-C-A

132631989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764230-C-T

132632192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28764012-G-A

132632271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28763906-C-T

http://identifiers.org/hco/9/GRCh38#132632576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28763302-C-A

132632947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28762958-C-T

132633216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28762556-A-G

132633835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28762051-G-A

132636676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28758501-C-T

132636966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28758213-C-T

132637231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28758033-A-G

http://identifiers.org/hco/9/GRCh38#132637302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28757961-C-A

132637348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28757915-A-G

132637360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28757903-C-T

132637825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28757438-A-G

132637885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757383-T-C

132637905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757364-T-C

132638037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757229-T-A

132638037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757229-T-C

132638066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757202-G-A

132638066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757202-G-T

132638098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757167-C-T

132638129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757136-G-A

132638129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757136-G-T

http://identifiers.org/hco/9/GRCh38#132638186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28757098-C-A

132638212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757070-G-C

132638232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28757049-T-C

http://identifiers.org/hco/9/GRCh38#132638314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28756994-A-C

132638329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28756979-A-G

132638365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 28756942-T-C

132638627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28756611-T-C

132638945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28756304-A-T

132640051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28755326-C-T

132640079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28755300-C-G

132641180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28754743-T-C

http://identifiers.org/hco/9/GRCh38#132641936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28753980-A-C

132641984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28753826-G-T

132642094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28753650-A-G

http://identifiers.org/hco/9/GRCh38#132642138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28753586-C-A

132642152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28753574-T-G

132642184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28753539-T-G

132642219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28753503-T-A

132644716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28751898-A-G

http://identifiers.org/hco/9/GRCh38#132644771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28751850-C-A

132644771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28751850-C-T

132645354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28751390-G-C

132645781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750979-T-C

132646077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28750720-T-C

132646102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750699-C-T

132646177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750614-T-C

132646347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750479-C-T

132646505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750352-G-A

132646746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750160-C-T

132646762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750145-T-C

132646770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28750137-A-T

132646999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28749938-T-G

132647085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28749853-C-G

http://identifiers.org/hco/9/GRCh38#132647326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28749726-A-C

132648170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28749123-T-A

132648170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28749123-T-C

132648272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28749021-T-C

132648327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28748971-A-G

132648392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28748903-C-T

132648652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28748651-A-G

132648732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28748595-T-C

132649408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747936-G-A

132649602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747835-T-C

132649658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747784-A-G

132649658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747784-A-T

132649683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747751-C-T

132649820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747564-C-T

132650076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747339-T-G

132650106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28747316-T-G

http://identifiers.org/hco/9/GRCh38#132650219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28747209-C-A

132650450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28746971-A-G

132650450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28746971-A-T

132650460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28746966-C-T

132650908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28746493-G-A

http://identifiers.org/hco/9/GRCh38#132650965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28746350-C-A

132651061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28746260-A-G

132651377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28745963-A-G

132651416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28745934-T-C

132651427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28745923-G-A

132651765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28745660-T-G

132652101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28745157-A-G

132652121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28745137-C-T

http://identifiers.org/hco/9/GRCh38#132652366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28744906-C-A

132652369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28744903-G-A

http://identifiers.org/hco/9/GRCh38#132652386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28744884-A-C

132652434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28744839-G-A

132652434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28744839-G-C

132652476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28744797-T-C

132652515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28744761-T-C

132655137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28743104-A-G

132655174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28743068-T-C

132655227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28743015-T-A

132655269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28742973-A-G

132655269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28742973-A-T

132655546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28742661-T-C

132655582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28742630-G-C

132656192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28742064-T-C

http://identifiers.org/hco/9/GRCh38#132656269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28741998-C-A

132657948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28739027-A-G

132657953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28739022-T-A

132658002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738992-G-T

132658003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738991-T-C

132658075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738912-T-C

132658384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738616-G-C

132658384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738616-G-T

132658396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738604-A-G

132658396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738604-A-T

132658436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738569-G-A

132658436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738569-G-C

132658436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738569-G-T

132658476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738530-A-G

132658591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738442-C-T

132658713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28738318-G-T

http://identifiers.org/hco/9/GRCh38#132658860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28738215-C-A

132658860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28738215-C-G

132659446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737751-A-G

132659446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737751-A-T

132659615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737614-G-A

132659615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737614-G-C

132659615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737614-G-T

132659655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737577-T-A

132659660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737572-G-T

132659688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737542-G-A

132659688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28737542-G-T

132660191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28736997-T-C

132660302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28736933-T-A

132660362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28736916-A-G

http://identifiers.org/hco/9/GRCh38#132660823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28736397-C-A

132661005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28736231-G-A

132661064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28736173-G-A

132661096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28736155-G-A

132661096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28736155-G-C

132661109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28736136-A-G

132661337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735933-G-C

132661337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735933-G-T

http://identifiers.org/hco/9/GRCh38#132661390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28735882-C-A

132661390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735882-C-T

132661640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735733-G-A

132662138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735363-G-T

132662146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735355-A-G

132662146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735355-A-T

132662329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28735215-C-T

132662411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28735134-C-T

http://identifiers.org/hco/9/GRCh38#132662433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28735110-A-C

http://identifiers.org/hco/9/GRCh38#132663277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28734270-A-C

132663277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28734270-A-G

132663318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28734229-A-G

132663362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28734186-T-C

132663579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28733922-T-C

http://identifiers.org/hco/9/GRCh38#132663639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28733775-A-C

132664365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28733116-C-T

http://identifiers.org/hco/9/GRCh38#132664646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28732972-C-A

132664646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28732972-C-T

http://identifiers.org/hco/9/GRCh38#132664733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28732929-A-C

http://identifiers.org/hco/9/GRCh38#132664750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28732912-C-A

132669958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730769-G-A

132669958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730769-G-T

http://identifiers.org/hco/9/GRCh38#132670084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28730684-C-A

132670084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730684-C-T

132670087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730681-G-A

132670087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730681-G-C

132670174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730605-G-A

132670174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730605-G-C

132670174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730605-G-T

132670185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28730594-T-C

http://identifiers.org/hco/9/GRCh38#132670385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28730438-C-A

132670385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28730438-C-G

132670385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28730438-C-T