57994594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5644228-G-A

57994594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5644228-G-C

57994651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5644277-G-A

http://identifiers.org/hco/8/GRCh38#57994720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5644332-C-A

57994720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5644332-C-G

57994720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5644332-C-T

57994725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5644337-C-T

57994752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5644360-G-A

57994961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5644459-C-T

57995092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5644517-G-C

57995129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5644529-G-A

57995129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5644529-G-C

57995248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5644605-C-T

57995390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5644718-C-T

57995901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5645197-C-T

57996381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5645718-G-A

57996381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5645718-G-T

57996756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5646045-C-T

57996788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5646050-G-A

57997190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5646410-T-C

57997514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5646740-C-T

57997733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5646925-A-G

57997733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5646925-A-T

57997910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5647085-G-A

57997969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5647138-C-T

57998489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5647592-A-G

57998489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5647592-A-T

57998545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5647660-G-A

57998807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5647910-G-A

57999112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5648309-A-G

57999213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5648430-A-G

57999637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5648846-A-G

57999644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5648853-A-G

58000315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5652531-G-C

58000786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5653018-T-C

58000936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5653151-G-A

58000936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5653151-G-C

58000936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5653151-G-T

58001169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5653385-C-T

58001266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5659864-G-A

58001469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5660134-A-G

58009242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5663411-G-A

58009450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5663692-A-G

58013030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665012-G-T

58013047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665029-A-G

http://identifiers.org/hco/8/GRCh38#58013211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5665173-C-A

58013300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665269-A-G

58013327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665296-C-T

58013357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665324-T-C

58013430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665397-A-G

58013621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665597-G-A

58013679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665640-A-G

58013681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665642-T-G

58013709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665672-A-G

58013855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665836-C-G

58013999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5665983-G-A

58014648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5666693-T-C

58014657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5666702-T-C

58014980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5667038-C-G

http://identifiers.org/hco/8/GRCh38#58015876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5667284-C-A

58016130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5667535-G-A

58016245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5667657-T-A

58016483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5667817-A-G

58016527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5667858-C-T

58021479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5668333-C-G

58021772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5668712-A-G

http://identifiers.org/hco/8/GRCh38#58021888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5668951-A-C

58022093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5669125-G-T

http://identifiers.org/hco/8/GRCh38#58022322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5669358-A-C

58022322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5669358-A-G

58022328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5669364-G-C

58022458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5669495-G-A

58022659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5669690-T-C

58022907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5669939-C-T

58023336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5670595-T-C

58023336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5670595-T-G

58023780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5670924-A-G

http://identifiers.org/hco/8/GRCh38#58023848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5670994-C-A

58023848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5670994-C-T

http://identifiers.org/hco/8/GRCh38#58024224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5671353-C-A

58024224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671353-C-T

58024525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671642-A-G

58024578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671690-G-A

58024602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671714-G-A

58024654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671764-C-T

58024882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671964-T-C

58024910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5671992-A-G

58024988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5672099-C-T

58025001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5672110-G-A

58025046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5672169-A-G

58025503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5672586-T-C

58025803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5672900-A-G

58025831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5672928-C-T

58027537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5675181-C-T

http://identifiers.org/hco/8/GRCh38#58027542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5675186-A-C

58027629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5675263-A-G

58027714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5675348-G-C

58027723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5675357-T-A

58028049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5675665-T-G

58028705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5676280-A-G

58028755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5676321-G-A

58028868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5676428-G-A

58029107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5676593-C-T

58029697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5677092-C-G

58030020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5677393-T-C

58030074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5677449-T-G

58030252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5677611-G-A

58030252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5677611-G-C

58030564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5677933-G-A

58031122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5678455-A-G

58031184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5678512-A-G

58031211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5678535-T-C

58031289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5678611-G-T

58031313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5678636-G-T

58031433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5678719-G-C

58031433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5678719-G-T

http://identifiers.org/hco/8/GRCh38#58031483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5678770-C-A

58031483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5678770-C-T

58031580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5678877-T-A

58031674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5678969-G-T

58031761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679056-T-C

58031761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679056-T-G

58031832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679121-T-C

58031882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679171-T-C

58031964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679249-C-T

http://identifiers.org/hco/8/GRCh38#58032004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5679287-C-A

58032004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679287-C-T

58032050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679318-A-G

58032065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679334-G-A

58032065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679334-G-T

58032073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679342-T-C

58032074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679343-G-T

http://identifiers.org/hco/8/GRCh38#58032111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5679384-C-A

58032189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5679452-T-C

58032224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5679491-C-T

58034712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679771-G-A

58034746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5679803-T-C

58035277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5680320-T-C

58035508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5680674-G-T

58035526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5680698-G-T

58035553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5680729-C-G

58035559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5680735-C-T

58036229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5681347-G-A

58036340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5681449-C-T

58036374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5681487-T-A

58036374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5681487-T-C

58036380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5681493-T-C

58036504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5681613-T-C

58036591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5682161-A-G

58037836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684058-T-C

58037864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684069-C-T

58037901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684105-T-C

58037948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684151-A-G

58037991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684193-G-A

58038170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684354-G-A

58038205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684389-C-T

58038360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684542-T-A

58038879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684757-A-G

58038879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684757-A-T

58038993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684842-A-G

58039015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5684864-T-C

58039238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5685140-G-A

http://identifiers.org/hco/8/GRCh38#58039333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5685224-C-A

58039368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5685257-C-T

58039396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5685286-G-A

58039615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5685526-C-T

58040405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5685865-G-A

58041644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5688024-A-G

58041716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5688093-G-A

58042210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5688432-A-G

58042633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690066-A-G

58042643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690075-C-T

58042671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690102-G-A

58042728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690157-G-A

58042885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690278-T-C

58043016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690387-G-A

58043058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690429-A-G

58043080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690447-C-T

58043109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690475-G-T

58043157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690522-G-T

58043243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5690606-G-T

58043403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5690731-C-T

http://identifiers.org/hco/8/GRCh38#58043413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5690741-C-A

58044914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5694493-A-G

58045290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5694808-C-T

58045297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5694815-C-G

58045466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5694995-T-C

58045509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5695040-T-C

58045673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5695175-G-A

58045733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5695278-A-G

58045770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5695375-A-G

58045867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5695587-C-T

http://identifiers.org/hco/8/GRCh38#58046249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5695942-A-C

58046356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5696147-T-C

58046644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5696454-G-A

http://identifiers.org/hco/8/GRCh38#58047420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5697234-A-C

58047420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697234-A-G

58047517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697321-C-T

58047630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697554-C-G

58047736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697632-G-A

58047741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697637-G-T

58047913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697783-G-C

http://identifiers.org/hco/8/GRCh38#58047936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5697806-C-A

58047936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697806-C-T

58048053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697901-T-C

58048068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697916-C-T

58048104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5697949-A-G

58049689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5698384-G-T

58049737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5698460-A-G

58049751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5698474-T-G

http://identifiers.org/hco/8/GRCh38#58050071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5698645-C-A

58050100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5698672-G-A

58050369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5698961-A-G

58050414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5698999-T-G

58050424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699009-G-A

58050520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699098-G-A

58050607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699180-A-G

58050607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699180-A-T

58050683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699217-G-A

58050787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699307-G-A

58050787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5699307-G-T

58051051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5700164-T-A

58051153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5700258-C-T

58051675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5700679-G-A

58051725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5700719-A-G

58052092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701060-T-G

58052122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701091-C-G

58052344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701318-G-T

http://identifiers.org/hco/8/GRCh38#58052401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5701372-A-C

58052401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701372-A-G

58052615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701547-A-G

58052755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701676-G-T

58052767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5701688-G-T

http://identifiers.org/hco/8/GRCh38#58052770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5701691-C-A

58055798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5702042-T-C

58055899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5702128-G-A

58055899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5702128-G-T

58055902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5702135-G-T

58056201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5702494-G-T

58056565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703080-C-T

58056694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703227-G-A

http://identifiers.org/hco/8/GRCh38#58056835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5703355-A-C

58056838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703358-C-T

58056936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703453-G-A

58056950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703467-G-A

58057108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703589-G-A

58057128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703607-G-A

58057170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703658-C-G

58057170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5703658-C-T

58057717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5704416-G-C

58057870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5704551-G-A

58057901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5704580-T-C

58057918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5704595-C-T

58058107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5704754-T-A

58060139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707150-G-C

58060161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707173-G-A

58060180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707192-A-G

58060271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707278-G-A

58060277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707284-G-A

58060400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707409-A-G

58060474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707491-C-T

58060783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707751-G-A

58060816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707774-A-G

58060955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5707907-G-A

58061234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5708485-A-G

58061413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5708634-T-C

58061533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5715420-G-A

58061802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5715663-C-T

58061835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5715689-C-T

58061853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5715709-T-C

58061948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5715794-A-G

58062147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5715987-A-G

http://identifiers.org/hco/8/GRCh38#58062198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5716037-C-A

58062429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5716767-G-A

58062472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5716812-A-G

58062472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5716812-A-T

58062486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5716826-C-T

58062556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5716897-T-C

58062626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5716968-G-T

58062663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5717006-G-A

58062712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5717055-G-T

58062720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5717063-T-G

58062757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5717100-C-T

58063153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5717492-C-T

58063194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5717606-C-T

58064464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5718704-G-A

58065332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5719468-T-A

58065585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5719692-T-G

58065635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5719741-A-T

58067221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5720992-T-A

58067472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5721672-C-T

58067607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5721798-G-A

58067607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5721798-G-T

58067618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5721809-C-T

58067671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5721873-C-T

58067702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5721903-A-G

58067872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5722097-C-T

58068057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5722272-G-A

58068077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5722292-G-T

http://identifiers.org/hco/8/GRCh38#58068591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5722742-C-A

58068816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5722937-G-A

58068821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5722941-G-A

http://identifiers.org/hco/8/GRCh38#58068848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5722969-C-A

58069326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723449-A-T

58069366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723491-G-T

58069378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723503-G-A

58069386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723510-G-A

58069483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723618-A-G

58069519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723654-T-G

58069629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723746-T-G

58069637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723754-C-T

58069648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723765-A-G

58069648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723765-A-T

58069729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723848-G-A

58069820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5723942-T-A

58070174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724290-C-T

58070501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724633-G-T

http://identifiers.org/hco/8/GRCh38#58070513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5724645-A-C

58070751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724852-G-A

58070751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724852-G-C

58070757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724858-G-A

58070765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724866-T-G

58070802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5724904-T-C

58071009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5725111-C-G

58071314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5725373-A-G

58071605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5725662-G-A

58071722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5725776-G-A

58071731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5725783-G-T

58071734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5725786-T-C

58072128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5726369-C-T

58072132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5726373-C-T

58072140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5726381-C-T

58072419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5726809-T-C

58072473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5726863-T-C

58072593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5726974-C-T

58072914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5727387-G-A

58072941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5727415-T-A

58072941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5727415-T-C

58073180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5727658-A-G

58073442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5727891-A-G

58073495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5727934-G-A

58073711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728155-G-A

58073839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728297-A-G

58074020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728499-T-A

58074020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728499-T-G

58074066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728546-C-G

http://identifiers.org/hco/8/GRCh38#58074112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5728585-C-A

58074158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728652-C-G

58074235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728718-C-T

58074304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728770-C-T

58074357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728811-C-T

58074373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728817-A-T

58074400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5728844-C-T

58074597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729037-T-C

58074616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729056-G-A

58074955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729318-G-A

58074984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729345-G-C

58075450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729486-T-G

58075547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5729583-G-A

58075547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5729583-G-T

58075583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5729618-A-G

58075650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729684-A-G

58075675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5729709-C-G

58076322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730021-G-C

58076585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730267-C-T

58076594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730280-G-A

58076985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730664-G-A

58076985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730664-G-T

http://identifiers.org/hco/8/GRCh38#58077122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5730778-C-A

58077162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5730814-T-C

58077174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5730826-G-A

58077174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5730826-G-C

58077218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730870-G-A

58077218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730870-G-T

58077222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5730874-A-G

http://identifiers.org/hco/8/GRCh38#58077296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5730948-C-A

58077296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730948-C-G

58077296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5730948-C-T

58077346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731163-G-C

58077366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731231-G-A

58077740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731588-G-A

58077740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731588-G-T

58077861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731709-C-T

58077909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731757-C-G

58077978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5731832-A-G

58078261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5732172-G-A

58078287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5732207-G-T

58078336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5732257-G-A

58078460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5732379-T-C

58079146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5732737-C-T

58079232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5732825-A-G

58079833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5733443-A-G

58080078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5733675-T-C

58080177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5733744-C-T

58080266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5733829-A-G

58080396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5733952-G-A

http://identifiers.org/hco/8/GRCh38#58080487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5734029-C-A

58080556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5734099-A-G

58080709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5734250-G-A

58080735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5734276-A-G

58080744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5734285-A-G

58080752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5734293-C-T

58081664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5735132-A-G

58085872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738440-A-G

58085872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738440-A-T

58085938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738504-A-G

58087999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738558-C-T

http://identifiers.org/hco/8/GRCh38#58088111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5738645-A-C

58088113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738647-T-A

58088180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738701-G-A

58088193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738714-A-T

http://identifiers.org/hco/8/GRCh38#58088244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5738764-A-C

58088361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5738887-A-G

58088504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5739049-G-A

58088508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5739053-T-G

58088515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5739060-G-A

58088526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5739071-T-C

58088719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5739261-G-A

58088858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5739383-T-C

58089566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5740083-A-G

http://identifiers.org/hco/8/GRCh38#58089689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5740161-A-C

58089761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5740234-T-G

58089775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5740247-T-A

58089775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5740247-T-C

58090731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5740513-A-G

http://identifiers.org/hco/8/GRCh38#58091354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5741083-C-A

58091354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741083-C-T

58091355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741084-T-C

58091386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741115-C-G

http://identifiers.org/hco/8/GRCh38#58091462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5741189-C-A

58091462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5741189-C-T

http://identifiers.org/hco/8/GRCh38#58091463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5741190-A-C

58091516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5741249-C-T

58091565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5741298-T-G

58091654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741387-G-A

58091722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741443-A-G

58091813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5741537-G-C

58091848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5741572-G-T

http://identifiers.org/hco/8/GRCh38#58091903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5741621-C-A

58091903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741621-C-G

58091924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741641-G-T

58091983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5741691-G-A

58099188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742096-G-A

58099546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742224-A-T

58101741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742392-A-G

58101825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742477-C-T

58101843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742495-C-T

58101878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742538-T-C

http://identifiers.org/hco/8/GRCh38#58101895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5742555-A-C

58101987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742616-C-G

58102011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742638-G-C

58102092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742701-T-G

58104087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742837-A-G

58104111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742861-A-G

58104149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5742896-C-T

58104549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5743776-A-G

58104637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5743855-T-C

58104639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5743857-T-C

58104687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5743905-T-G

58104865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744073-A-G

http://identifiers.org/hco/8/GRCh38#58105156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5744321-C-A

58105325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744478-G-A

58105345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744498-T-C

58105895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744541-G-A

58105895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744541-G-T

58106103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5744759-A-G

http://identifiers.org/hco/8/GRCh38#58106107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5744763-C-A

58106253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5744895-G-T

http://identifiers.org/hco/8/GRCh38#58106377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5745019-A-C

58106377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745019-A-G

58106448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745100-C-T

58106534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745185-C-G

58106534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745185-C-T

58106535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5745186-G-A

58107209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5746570-C-T

58107294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5746657-T-G

58107369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5746721-A-T

58107579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5746913-G-A

58107938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5747204-A-G

58107939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5747205-G-A

58108052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5747300-G-A

58109326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749183-A-G

58109336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749193-T-A

58109367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749223-G-C

58109509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749369-G-A

58109529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749389-C-T

58109748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749580-G-A

58109867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749699-T-C

58109875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5749707-A-T

58110297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5750105-G-A

58110313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5750121-A-T

58110497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5750287-T-C

58110628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5750419-G-T

58110679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5750465-A-G

http://identifiers.org/hco/8/GRCh38#58110808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5751128-C-A

58110930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5751212-T-C

58111098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5751377-T-C

58111395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5751664-C-T

58111403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5751672-G-A

58111574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5751809-C-T

58112523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5752673-C-T

58112677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5752792-T-A

58112677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5752792-T-G

http://identifiers.org/hco/8/GRCh38#58112817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5752923-A-C

58112964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753019-T-C

58113031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753080-G-A

58113031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753080-G-C

http://identifiers.org/hco/8/GRCh38#58113047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5753096-C-A

58113690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753183-T-A

58113710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753203-A-G

58113736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753231-A-G

58113783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753278-A-G

58113789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753283-G-A

58113820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753314-C-T

58113895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753389-A-G

58113910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753397-A-G

58114052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753531-A-G

58114161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753648-T-C

http://identifiers.org/hco/8/GRCh38#58114270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5753735-A-C

58114332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753798-T-C

58114433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753891-C-T

58114444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5753905-G-A

58114561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5754004-A-G

http://identifiers.org/hco/8/GRCh38#58115166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5754765-C-A

58116840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5755674-G-A

58116893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5755732-T-A

58116934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5755774-T-C

58116965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5755804-G-A

58117043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5755884-G-C

58117244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5756079-C-T

58117428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767671-G-C

58117473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767715-C-T

58117512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767747-G-A

58117525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767760-G-T

58117565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5767784-C-T

58117989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768210-C-G

58117989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768210-C-T

58118224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5768383-G-C

58118281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5768435-T-C

58118359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5768918-G-A

58118431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5768991-A-G

58118590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769620-C-G

58118610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769640-A-T

58118929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5769946-G-T

58119154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770124-T-C

58119213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770183-C-G

58119290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770441-G-A

58119303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770456-G-A

58119372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770507-A-G

58119560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770707-A-G

http://identifiers.org/hco/8/GRCh38#58119562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5770709-A-C

58119755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770921-G-A

http://identifiers.org/hco/8/GRCh38#58119777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5770940-C-A

58119777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5770940-C-T

58119948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771123-A-G

58119971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771146-C-T

58120012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771186-C-T

58120057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771260-G-A

58120057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771260-G-C

58120123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771353-A-G

58120164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771394-G-T

58120213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771422-T-C

58120519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771571-A-T

58120787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771849-G-T

58120801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771863-A-G

http://identifiers.org/hco/8/GRCh38#58120876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5771927-A-C

58121077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5772150-A-T

58121531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5772597-T-C

58121629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5772672-A-G

58122209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773222-C-T

58122369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773355-C-T

http://identifiers.org/hco/8/GRCh38#58122474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5773452-A-C

58122601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773570-G-A

58122755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773714-G-C

58122809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773768-G-T

58123108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774045-T-C

58123217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774115-G-A

58123315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774224-G-C

58123967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775163-G-A

58124173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775347-T-C

58124189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775363-C-T

58124223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775396-C-T

58124285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775457-C-T

58124391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775538-C-T

58124578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775702-G-C

58124705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775846-A-G

58124745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5775869-C-T

58126938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5777138-C-T

58126945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5777145-T-C

58126979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5777178-C-G

58126979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5777178-C-T

58128085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5778568-C-T

58128136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5778609-G-A

58128349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5778845-G-C

58128846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5779422-A-G

58128899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5779470-G-T

http://identifiers.org/hco/8/GRCh38#58129010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5779579-A-C

58129109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5779678-T-G

58129139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5779708-A-G

58129164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5779733-G-A

58129201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5779772-T-A

58129747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5780293-G-T

58129866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5780355-A-T

58129884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5780371-A-G

58129975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5780465-T-C

58130057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5780552-C-T

58130209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5780674-T-G

http://identifiers.org/hco/8/GRCh38#58130451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5781329-C-A

http://identifiers.org/hco/8/GRCh38#58130627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5781455-A-C

http://identifiers.org/hco/8/GRCh38#58130653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5781481-A-C

58130653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781481-A-G

58130714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781531-A-G

58130781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781600-G-A

58130785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781604-G-A

58130785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781604-G-C

58130864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781680-G-T

58130870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781686-G-A

58130873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781689-A-T

58130893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781709-G-A

58130893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781709-G-C

58130928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781758-G-A

58130929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781759-C-T

58130930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781760-G-A

http://identifiers.org/hco/8/GRCh38#58130958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5781788-C-A

58130988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781823-G-A

58130994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781828-C-G

58131129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781917-A-G

58131155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5781942-A-G

58131224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5782009-T-C

http://identifiers.org/hco/8/GRCh38#58131579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5782400-A-C

58131684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5782505-A-G

58131706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5782510-T-A

58131706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5782510-T-G

58131840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5782643-A-G

58131895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5782680-T-A

http://identifiers.org/hco/8/GRCh38#58132195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5782994-C-A

58132219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783018-C-T

58132422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783143-T-C

58132447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783156-C-T

58132452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783161-T-A

58132489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783179-T-C

58132491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783181-G-A

58132684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783342-C-T

58132696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783354-G-T

58132719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783377-T-C

58132780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783427-C-T

58132781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783428-A-G

58132781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783428-A-T

58132810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783459-A-T

58132927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783539-G-A

http://identifiers.org/hco/8/GRCh38#58133118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5783708-A-C

58133128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783724-G-T

58133167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783771-T-G

58133191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783795-G-T

58133202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5783806-T-A

http://identifiers.org/hco/8/GRCh38#58133297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5784158-A-C

58133355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784212-C-T

58133488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784290-G-A

58133700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784456-A-G

58133715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784471-T-G

58133718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784474-T-A

58133739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784491-A-T

58133758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784517-C-T

58134144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5784963-A-G

58134358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5785230-G-A

58134403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5785269-T-C

58134495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5785358-T-G

http://identifiers.org/hco/8/GRCh38#58135194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5785964-A-C

58135194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5785964-A-G

58135355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786078-G-C

58135596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786282-G-A

http://identifiers.org/hco/8/GRCh38#58136412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5786697-C-A

58136524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786797-A-G

58136575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786852-T-C

58136626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786893-C-T

58136667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786931-C-G

58136667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5786931-C-T

58136827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5787071-C-T

58136882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5787115-C-G

http://identifiers.org/hco/8/GRCh38#58136923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5787154-C-A

58136923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5787154-C-T

58137135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5787387-G-T

http://identifiers.org/hco/8/GRCh38#58137285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5787556-C-A

58137705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5787816-C-T

58137781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5787899-A-G

58137988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788105-A-G

58137997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788124-A-G

58137997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788124-A-T

58138043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788170-C-T

58138112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788240-C-G

58138112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788240-C-T

58138160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788286-T-C

58138280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788404-G-A

58138401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788544-G-C

58138521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5788655-C-G

http://identifiers.org/hco/8/GRCh38#58138943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5789375-C-A

58139207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790222-T-A

58139207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790222-T-C

58139495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790498-A-G

58139506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790509-G-C

58139506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790509-G-T

58139529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790548-G-A

58139536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790555-C-T

58139551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790570-C-T

58139621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5790997-A-G

http://identifiers.org/hco/8/GRCh38#58139643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5791017-A-C

58139675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5791049-A-G

58141177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793473-A-T

58141263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793655-G-A

58141263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5793655-G-T

58141621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794006-G-A

58141783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5794134-C-T

58141809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794158-C-G

58142277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794530-C-T

58142340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794589-C-T

58142567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794706-T-A

58142567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794706-T-C

58142595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794728-T-C

58142747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5794840-A-T

58143133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5795342-A-G

58143166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5795362-C-T

58143437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5795562-G-A

http://identifiers.org/hco/8/GRCh38#58143458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5795580-A-C

58143737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5795854-A-T

58143862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5795991-C-T

58143910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5796043-A-T

58144010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5796139-G-A

58144077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5796200-G-A

58144444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797026-C-T

58145296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797609-A-G

58145313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797626-A-T

58145339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797652-G-T

58145367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5797680-C-T

58145665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798008-C-T

58145722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798068-G-A

58145722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798068-G-T

58145764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798109-G-A

58145764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798109-G-T

http://identifiers.org/hco/8/GRCh38#58145817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5798179-C-A

58145817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798179-C-T

58145893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5798255-G-T

58146005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5798368-G-A

58146005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5798368-G-C

58146005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5798368-G-T

58146024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5798387-G-A

58146024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5798387-G-T

58146039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5798402-A-G

58146078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5798441-G-A

58146078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5798441-G-T

58146099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5798462-G-A

58146099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5798462-G-T

58146413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5798766-C-T

58146446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5798799-G-A

58146533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5798886-C-T

58146581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5798934-G-A

58146581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5798934-G-C

58146635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5798988-G-A

58146665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5799018-G-A

58146665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5799018-G-T

58146708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5799058-G-A

58146708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5799058-G-C

58146708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5799058-G-T

58146768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5799118-C-T

58146779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5799129-G-A

58146912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5799262-C-T

http://identifiers.org/hco/8/GRCh38#58147568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5799907-A-C

58147568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5799907-A-G

58147703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800050-T-A

58147703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800050-T-G

http://identifiers.org/hco/8/GRCh38#58147759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5800106-C-A

58147766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800113-A-G

http://identifiers.org/hco/8/GRCh38#58147875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5800222-C-A

58147969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800308-A-G

58148166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800509-G-T

58148187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800530-G-T

http://identifiers.org/hco/8/GRCh38#58148199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5800542-C-A

58148247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800591-G-A

58148247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800591-G-C

58148263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800607-G-A

58148263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800607-G-T

58148291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800635-C-T

58148360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800693-T-C

58148371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800713-T-A

58148421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800763-A-G

58148449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800791-G-A

58148449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800791-G-T

58148481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800815-T-C

58148514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5800831-T-C

http://identifiers.org/hco/8/GRCh38#58148647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5800971-A-C

58148864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801179-A-G

58149013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801334-C-G

58149130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801451-C-G

58149130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801451-C-T

58149242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801523-T-C

58149339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801614-A-G

58149700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801958-G-A

58149700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801958-G-C

58149700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5801958-G-T

58149756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802005-A-G

http://identifiers.org/hco/8/GRCh38#58149784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5802033-C-A

58149784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802033-C-T

58150097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802281-T-C

http://identifiers.org/hco/8/GRCh38#58150448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5802541-C-A

58150694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802758-G-C

58150748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802811-C-G

58150875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802933-G-T

58150891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802949-G-A

58150892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802950-C-T

58150893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802951-G-A

58150893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802951-G-T

58150912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5802993-C-T

58151702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5804568-G-T

58151715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5804581-T-C

58152236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5805074-C-T

58152437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5805274-G-A

58152659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5805481-C-T

58152687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5805508-C-T

58153008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5805790-G-A

58153061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5805833-G-A

http://identifiers.org/hco/8/GRCh38#58153068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5805840-C-A

http://identifiers.org/hco/8/GRCh38#58153146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5805914-C-A

58153342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806097-A-T

58153966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806668-G-A

58153966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806668-G-C

58153970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806672-C-G

58153970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806672-C-T

58153972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806674-A-T

http://identifiers.org/hco/8/GRCh38#58154164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5806821-A-C

58154216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5806866-T-C

58156257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807265-G-A

58156323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807323-C-T

58156326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807326-G-T

58156400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807402-C-G

http://identifiers.org/hco/8/GRCh38#58156440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5807445-C-A

58156440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807445-C-T

58156572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807555-G-T

http://identifiers.org/hco/8/GRCh38#58156632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5807615-A-C

58156645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807628-A-T

58156861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807825-G-C

58156861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5807825-G-T

58157224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5808231-A-G

58158205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5808575-G-T

58158277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5808641-G-A

58158348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5808716-C-T

http://identifiers.org/hco/8/GRCh38#58158471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5808817-A-C

58158518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5808847-G-A

58158775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809070-T-C

58159153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809377-G-C

58159192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809412-C-T

58159271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809547-C-G

58159348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809623-C-T

58159360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809635-T-C

58159391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809666-G-A

58159391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809666-G-T

58159790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5809826-C-T

58160589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5810458-G-A

58160772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5810897-G-A

58160876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811006-T-C

58160921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811102-G-A

58160948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811128-G-T

58161485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811439-T-G

58161528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811459-G-C

58161528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811459-G-T

58161572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811503-T-C

58161620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811551-A-G

58161864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811795-C-T

58162054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5811992-T-C

58162113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5812048-C-T

58162166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5812105-T-C

58162759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5814462-G-A

http://identifiers.org/hco/8/GRCh38#58162920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5814623-C-A

58163656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5815039-G-A

http://identifiers.org/hco/8/GRCh38#58163681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5815085-C-A

58163737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5815145-A-G

58163941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5815644-T-C

58163942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5815645-A-G

58164306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5816324-A-G

58164340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5816357-T-G

58164512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5816530-G-A

58164512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5816530-G-T

58164884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5816938-A-G

58167839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5826199-A-G

58167966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5826324-A-G

http://identifiers.org/hco/8/GRCh38#58168013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5826371-C-A

http://identifiers.org/hco/8/GRCh38#58168033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5826391-C-A

58168061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5826414-T-C

58168155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5826466-A-G

58168181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5826491-C-G

58168355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5826674-G-A

58169561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5827589-G-A

58169668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5827692-C-G

58169669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5827693-C-T

58169932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5827916-T-C

58170898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5829234-C-T

58170912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5829248-G-A

58171010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5829514-G-T

58171404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5829906-A-G

58171509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830011-G-C

58171713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830211-A-G

58171713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830211-A-T

58171773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830261-T-A

58172042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830513-T-C

58172126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830592-C-T

58172253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830718-G-A

http://identifiers.org/hco/8/GRCh38#58172279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5830734-A-C

58172338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830788-G-A

58172484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5830948-A-G

58174789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5836630-T-G

58175218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5837081-C-T

58175312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5837172-G-T

58175613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5837437-T-C

58175630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5837454-G-C

58181306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5847195-A-G

http://identifiers.org/hco/8/GRCh38#58181598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5847502-C-A

58181598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5847502-C-G

http://identifiers.org/hco/8/GRCh38#58181625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5847529-C-A

58181625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5847529-C-T

58182103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5847824-A-T

http://identifiers.org/hco/8/GRCh38#58182464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5847961-C-A

58184292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5852417-T-C

58185419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856268-T-G

58185483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856331-C-T

58185543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856546-G-T

58185561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856564-G-T

http://identifiers.org/hco/8/GRCh38#58185894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5856897-A-C

58185894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856897-A-G

58185929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856942-A-G

58185965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5856976-G-C

58186003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5857011-A-G

58186025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5857031-G-A

58186025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5857031-G-C

58186037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5857043-C-T

58186559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5861904-A-T

58186600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5861951-G-T

58186643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5861971-G-A

58186686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5862007-G-A

http://identifiers.org/hco/8/GRCh38#58186710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5862029-A-C

58186710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5862029-A-T

58187168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5862843-A-G

58187623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5863859-A-G

58187819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5864065-T-G

58187851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5864096-A-G

58188013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5864255-C-T

58188148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5864389-A-G

58196877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5885920-A-G

58196956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5885985-G-A

58196986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5886015-C-T

58197176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5886185-T-A

http://identifiers.org/hco/8/GRCh38#58197232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5886238-A-C

58197691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5887271-T-C

58197792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5887370-T-A

58197810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5887392-T-C

58197889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5887471-T-C

http://identifiers.org/hco/8/GRCh38#58198003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5887580-C-A

58198003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5887580-C-T

58203618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903653-A-T

58203671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903703-A-G

58203749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903756-C-T

http://identifiers.org/hco/8/GRCh38#58203867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5903872-C-A

58203884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903889-T-C

58203906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903910-T-C

58203936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903946-C-T

58203937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903948-T-A

58203937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903948-T-C

58203938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903949-G-C

http://identifiers.org/hco/8/GRCh38#58203995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5903996-C-A

58203995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5903996-C-T

http://identifiers.org/hco/8/GRCh38#58204122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28587
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#5904096-A-C