50067889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 116184998-T-C

50067924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 116185034-T-C

50067924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 116185034-T-G

50067991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 116185071-A-G

50068095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 116185158-T-C

50068243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116185305-C-G

50068243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116185305-C-T

http://identifiers.org/hco/10/GRCh38#50068356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116185357-C-A

50069523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116185892-C-T

50069791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186164-C-T

50070077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186444-T-C

50070244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116186807-T-C

50071693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116188219-A-G

50071726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116188250-G-A

50072814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116188639-A-G

http://identifiers.org/hco/10/GRCh38#50073131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116188950-C-A

50080657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116192938-T-G

50080729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116192978-A-G

50080868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116193117-A-G

50080940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193188-A-G

50080940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193188-A-T

50080972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193208-T-C

50081090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193311-G-A

50081090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193311-G-C

50081090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193311-G-T

50081216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193408-T-G

50081244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193436-T-A

50081244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116193436-T-G

50083939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194579-G-C

50083939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194579-G-T

50084014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194653-C-T

50084234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194875-T-C

50084254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194895-A-G

50084260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194901-A-G

http://identifiers.org/hco/10/GRCh38#50084267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116194906-C-A

50084267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194906-C-T

50084278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194916-T-C

50084278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194916-T-G

50084337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116194969-C-T

50085231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116195415-T-G

50085318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116195464-C-T

50085397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116195525-A-G

50085401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116195529-T-C

50085485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116195610-T-C

http://identifiers.org/hco/10/GRCh38#50085597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116195719-C-A

http://identifiers.org/hco/10/GRCh38#50085727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116195822-C-A

50085727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116195822-C-T

50086161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116196362-A-G

50086240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116196436-C-T

50086430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116196592-T-C

50086902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116196619-A-G

http://identifiers.org/hco/10/GRCh38#50087178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116196848-C-A

50087178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116196848-C-T

50087308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116196947-A-G

50087419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197149-G-T

50090574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197327-T-C

50090577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197330-A-G

50090577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197330-A-T

50090623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197372-C-T

http://identifiers.org/hco/10/GRCh38#50090688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116197411-C-A

50090709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197432-A-T

50090716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116197439-A-G

50090853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116197572-A-G

http://identifiers.org/hco/10/GRCh38#50090970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116198316-C-A

50090970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198316-C-T

50091001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198342-T-C

http://identifiers.org/hco/10/GRCh38#50091027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116198367-C-A

50091030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198378-C-G

50091050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198398-C-T

50091172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198523-A-G

50091178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198529-A-G

50091250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116198583-T-C

50091427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 116198773-G-A

50091500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116198840-G-A

50091500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116198840-G-C

50091500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116198840-G-T

50091821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116199886-G-A

50091936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116199973-T-C

50091941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116199978-A-G

50091941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116199978-A-T

50092033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200016-G-A

50092033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200016-G-T

http://identifiers.org/hco/10/GRCh38#50092050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200033-C-A

http://identifiers.org/hco/10/GRCh38#50092068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200051-C-A

50092068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200051-C-G

50092081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200064-G-A

50092081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200064-G-T

http://identifiers.org/hco/10/GRCh38#50092087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200069-C-A

50092087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200069-C-G

50092087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200069-C-T

50092155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 116200138-C-T

http://identifiers.org/hco/10/GRCh38#50092196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116200176-A-C

50092196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116200176-A-G

50092348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200287-G-A

50092348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200287-G-C

50092348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116200287-G-T

http://identifiers.org/hco/10/GRCh38#50093236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201354-C-A

http://identifiers.org/hco/10/GRCh38#50093300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201414-C-A

50093300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 116201414-C-G

50093395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201504-A-G

http://identifiers.org/hco/10/GRCh38#50093421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201521-C-A

50093440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201541-A-G

50093440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201541-A-T

50093452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201550-T-A

50093452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201550-T-C

50093452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201550-T-G

50093453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201551-A-G

50093477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201572-A-G

http://identifiers.org/hco/10/GRCh38#50093502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116201593-C-A

50093502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201593-C-G

50093535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201623-A-G

50093535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201623-A-T

50093569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201657-A-G

50093573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201661-T-C

50093663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201753-T-C

50093692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116201776-T-G

50093898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 116201975-T-A

http://identifiers.org/hco/10/GRCh38#50093934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116202008-C-A

50093934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116202008-C-G

50093934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116202008-C-T

50093947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116202021-G-A

50093947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116202021-G-C

50093947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116202021-G-T

http://identifiers.org/hco/10/GRCh38#50095158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116203398-A-C

50095557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204270-C-T

50095564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204277-T-C

50095566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204279-A-T

50095659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 116204367-A-T

http://identifiers.org/hco/10/GRCh38#50095738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116204455-C-A

50095738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 116204455-C-T

50095858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204568-C-G

50095858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204568-C-T

50095887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204597-C-T

50096109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204817-T-C

50096289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116204952-C-T

50096638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116205214-T-C

50096646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116205222-A-G

50097275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116205685-G-T

50097450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116205836-C-T

50097503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116205957-T-G

50097627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116206115-T-C

50097659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116206167-T-C

http://identifiers.org/hco/10/GRCh38#50097712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116206221-A-C

50097773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 116206282-G-A

50097925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116206794-T-C

50098100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116206926-T-C

50098136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116206961-C-G

50098136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116206961-C-T

50098247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116207056-C-T

50099693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116207813-C-T

50099859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116208406-A-G

50102582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116212273-G-C

50102591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116212282-C-T

50102703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116212394-C-G

http://identifiers.org/hco/10/GRCh38#50102742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116212431-A-C

50103618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116212730-A-G

http://identifiers.org/hco/10/GRCh38#50103826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116212905-C-A

50103898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116212940-C-T

50104090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 116213106-C-T

50104157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116213173-T-C

50104223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116213233-A-G

50105529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116213772-T-A

50105556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116213798-C-T

50105677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116214115-C-T

50105973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116214508-G-A

50106324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215083-G-C

50106475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215234-G-A

50106475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215234-G-C

50106494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215251-G-A

50106494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215251-G-T

50106541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215299-T-C

50106559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215317-C-T

http://identifiers.org/hco/10/GRCh38#50106590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116215349-C-A

50106590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215349-C-G

50106590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116215349-C-T

50110151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116218458-G-T

http://identifiers.org/hco/10/GRCh38#50110235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116218548-C-A

50110235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116218548-C-G

50110235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116218548-C-T

50111226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116219427-G-A

50111231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116219432-T-C

50111356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116219555-G-C

50111524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116219691-C-T

50111542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116219709-A-G

50111542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116219709-A-T

50112400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 116220328-G-A

50112409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 116220337-G-A

50112423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220351-G-A

50112423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220351-G-T

50112549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220620-G-C

50112564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220632-G-T

50112617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220681-G-A

50112654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220714-A-G

50112670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220730-G-A

50112723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220786-A-G

50112742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220805-C-T

50112909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116220963-G-C

50112953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221008-T-C

50113429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221090-C-T

50113563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221222-C-T

50113606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221269-C-T

50113648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221310-G-A

50113885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221543-G-A

50113885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116221543-G-T

50113916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 116221572-G-T

50116603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222036-G-A

50116608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222041-C-T

50117232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222537-G-A

50117341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222640-T-G

http://identifiers.org/hco/10/GRCh38#50117441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116222731-A-C

50117441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222731-A-G

50117742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222907-G-A

50117824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116222990-T-G

50117838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223004-G-A

50117838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223004-G-C

50117842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223008-A-G

50117842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223008-A-T

http://identifiers.org/hco/10/GRCh38#50117969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116223129-C-A

50117969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 116223129-C-T

50117974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116223134-T-C

50117974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116223134-T-G

50117976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116223136-G-T

50117992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116223152-T-G

50118092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223262-T-C

50118113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223285-A-G

50118161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223363-C-G

50118173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223375-G-T

50118232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223542-C-T

50118276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223640-G-T

50118305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223687-C-T

50118386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223795-G-C

50118386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116223795-G-T

50118690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116224081-G-T

50119018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116224381-C-T

50119082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116224470-C-T

50119189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116224563-T-C

50119190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116224564-A-G

50119603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 116224953-G-A

http://identifiers.org/hco/10/GRCh38#50119750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116225100-C-A

50119803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116225186-G-A

50119917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116225295-G-A

50119917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116225295-G-T

50120085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116225404-T-A

50120085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116225404-T-C

50125023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231011-A-G

50125029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231017-G-A

50125259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231208-C-G

50125295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231254-C-T

http://identifiers.org/hco/10/GRCh38#50125301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116231260-A-C

50125315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231320-T-C

50125348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231353-C-T

50125357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231362-T-A

50125357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231362-T-C

50125464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231469-T-C

50125586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231563-T-C

50125593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231570-A-G

50125615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231582-C-T

50125637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231597-T-C

http://identifiers.org/hco/10/GRCh38#50125654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116231608-A-C

http://identifiers.org/hco/10/GRCh38#50125727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116231666-A-C

http://identifiers.org/hco/10/GRCh38#50125844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116231816-A-C

50125844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231816-A-G

50126022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231976-T-A

50126022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231976-T-C

50126029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116231983-G-C

50126093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116232046-T-A

50126196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, stop_retained_variant
orthologous variants: 116232146-A-G

50126208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116232158-C-T

50126472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116232374-T-A

50126472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116232374-T-C

50126618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116232512-T-A

50126618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116232512-T-G

http://identifiers.org/hco/10/GRCh38#50126646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116232585-C-A

50126646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116232585-C-G

50126646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116232585-C-T

50126710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116232685-C-T

http://identifiers.org/hco/10/GRCh38#50127075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116233094-C-A

50127096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116233124-G-T

50127276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116233306-T-C

50127753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116233747-T-C

50127876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116233859-T-C

50127876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116233859-T-G

50128511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116234252-C-G

50129065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116234871-G-T

50129255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116235296-C-T

50129272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116235324-A-G

50129385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116235571-C-T

50129596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 116235786-G-A

50129706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 116235890-G-A

50129821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116235999-G-A

http://identifiers.org/hco/10/GRCh38#50129832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116236010-A-C

50129832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116236010-A-G

50129856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116236034-A-G

50129875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116236053-G-C

50129941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116236119-G-A

50129941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116236119-G-T

50130456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237050-T-A

50130546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237144-C-G

http://identifiers.org/hco/10/GRCh38#50130601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116237185-A-C

50130761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237330-T-C

50130831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237382-G-A

50130944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116237495-C-T

50131074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116237625-T-C

50131159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237689-C-T

50131252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237774-A-G

50131405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116237913-C-T

50131609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116238138-G-A

50131634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116238162-C-T

50132331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116238855-A-G

50132512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116239008-G-A

http://identifiers.org/hco/10/GRCh38#50132713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#116239205-A-C

50132713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116239205-A-G

50132783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116239273-G-A

50132783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 116239273-G-C

50132843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 116239333-C-G

50132859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 116239349-T-C

50133011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239511-G-A

50133222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239673-T-A

50133258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239712-G-A

50133258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239712-G-T

50133269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239722-G-T

50133338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239780-G-T

50133353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239795-G-A

50133353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 116239795-G-T

50133433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23416
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 116239877-C-T