http://identifiers.org/hco/7/GRCh38#50095931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11414100-A-C

50096140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: 11414322-A-G

50096140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: 11414322-A-T

50096148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11414330-A-T

50096160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11414348-G-A

50096318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: 11414506-A-G

50096326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: 11414514-C-T

50096337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, stop_gained
orthologous variants: 11414525-T-A

50096657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11414845-A-G

50096682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11414868-G-A

50096682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11414868-G-T

50096687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11414873-A-G

50096708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11414897-A-G

50096871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11415047-A-G

50097313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11415441-C-T

50097672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11416571-T-A

50097772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11416616-A-G

http://identifiers.org/hco/7/GRCh38#50098031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11416877-C-A

50098031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11416877-C-T

50098120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11416965-G-T

50103308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11418705-G-A

50103314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11418711-G-A

50103315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11418712-G-A

50103391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11418788-G-A

50103446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11418855-C-G

50103494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11418905-T-C

50103650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419051-C-G

50103680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419080-A-G

50103987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419398-A-G

50104051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419455-A-G

50104058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419462-T-C

50104065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419473-C-T

50104075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11419483-A-G

50104343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: 11427123-T-G

http://identifiers.org/hco/7/GRCh38#50104404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11427187-C-A

50104404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, missense_variant
orthologous variants: 11427187-C-T

50107396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11427846-G-A

50107396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11427846-G-C

50107396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11427846-G-T

50107954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11431432-T-C

50108222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11431696-T-C

50109216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432151-G-T

50109326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432254-T-G

http://identifiers.org/hco/7/GRCh38#50109790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11432373-A-C

50109790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432373-A-G

50109811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432407-G-C

50109852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432446-G-A

50109869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432463-G-A

50109890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11432481-A-G

50129678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11437634-A-G

http://identifiers.org/hco/7/GRCh38#50134060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11438468-C-A

50134065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438473-G-A

50134065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438473-G-T

50134066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438474-A-G

50134172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: synonymous variant
orthologous variants: 11438572-T-C

http://identifiers.org/hco/7/GRCh38#50134232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11438632-C-A

50134232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: missense variant
orthologous variants: 11438632-C-T

50134319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438718-A-G

http://identifiers.org/hco/7/GRCh38#50134372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11438736-A-C

50134372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438736-A-G

50134372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438736-A-T

50134377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438741-A-T

50134564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11438880-A-G

50134809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439125-C-T

50135454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439622-A-G

50135513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439678-G-A

50135596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439756-C-T

50135697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439847-C-T

50135748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439898-G-A

50135748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439898-G-C

50135835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11439965-G-A

50135892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440013-G-C

50136036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440156-T-A

50136036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440156-T-G

50136202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440313-C-T

http://identifiers.org/hco/7/GRCh38#50136205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11440316-A-C

50136205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440316-A-G

50136218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440328-G-A

50136272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440375-T-C

50136291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440394-T-C

50136579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440533-A-G

50136669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440619-A-G

50136892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440828-G-A

50136903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440841-T-C

50136923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440860-C-T

50136947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440880-T-C

http://identifiers.org/hco/7/GRCh38#50136956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11440888-C-A

50137054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440977-C-G

50137054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440977-C-T

50137058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11440981-T-C

50137343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11441114-A-G

50137343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11441114-A-T

http://identifiers.org/hco/7/GRCh38#50137392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11441163-C-A

50137448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11441217-A-T

50137486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11441255-C-T

50137528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11441300-A-G

50140045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445323-G-A

50140045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445323-G-T

http://identifiers.org/hco/7/GRCh38#50140176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11445451-C-A

50140176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 11445451-C-G

50140191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445466-G-A

50140191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445466-G-T

50140261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445525-T-C

50140448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445669-A-G

50140517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445742-G-A

50140552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445758-A-T

50140740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445930-C-T

50140778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11445962-G-T

50140849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11446031-C-T

50140884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11446058-C-G

50140884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11446058-C-T

http://identifiers.org/hco/7/GRCh38#50140966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11446141-C-A

http://identifiers.org/hco/7/GRCh38#50141260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11446380-C-A

50141266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11446386-T-C

50141281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 11446401-T-C

50141281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: missense_variant, splice_region_variant, synonymous_variant
orthologous variants: 11446401-T-G

http://identifiers.org/hco/7/GRCh38#50141450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11446556-C-A

50141450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11446556-C-G

50141516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11446623-G-T

http://identifiers.org/hco/7/GRCh38#50141584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11446689-C-A

50141584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11446689-C-G

50141584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11446689-C-T

http://identifiers.org/hco/7/GRCh38#50142037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11449675-C-A

50142055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11449693-C-G

50142062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11449700-G-A

50142062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11449700-G-C

50142062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11449700-G-T

http://identifiers.org/hco/7/GRCh38#50142079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11449722-C-A

http://identifiers.org/hco/7/GRCh38#50142110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11449752-C-A

50142324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11449960-G-C

50142440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11450076-A-T

http://identifiers.org/hco/7/GRCh38#50142669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11450272-C-A

50142693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11450302-C-G

50142739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11450346-G-A

50142739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11450346-G-T

http://identifiers.org/hco/7/GRCh38#50142772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11450375-C-A

http://identifiers.org/hco/7/GRCh38#50142810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#11450411-C-A

50142810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, undefined
orthologous variants: 11450411-C-G

50143115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11450731-T-C

50143115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11450731-T-G

http://identifiers.org/hco/7/GRCh38#50144551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11452068-C-A

50144616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11452137-T-C

http://identifiers.org/hco/7/GRCh38#50144869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11452465-A-C

50146985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11454720-G-T

50147007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11454742-G-A

50147062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11454797-G-A

50147062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11454797-G-T

50147391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11455087-T-C

50147568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11455237-T-C

50147619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11455306-T-A

50147863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11455672-G-A

50148103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11455916-G-A

50148103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11455916-G-C

50148291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11456132-T-C

50148454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11456300-T-C

50148484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11456329-C-T

50149218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11456740-G-A

50149685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11457084-G-A

50149710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11457109-G-A

50149900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11457283-G-A

http://identifiers.org/hco/7/GRCh38#50149995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11457378-C-A

50150123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458047-A-G

50150202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458120-T-C

50150318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458223-G-A

50150353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458261-A-T

50150446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458321-A-G

50150492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458361-G-A

50150869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458711-G-A

50151047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458867-G-A

50151065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458885-G-C

50151143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11458937-C-G

http://identifiers.org/hco/7/GRCh38#50151182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11458981-A-C

50151226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459028-G-A

http://identifiers.org/hco/7/GRCh38#50151269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11459063-C-A

50151269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459063-C-T

50151270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459064-G-A

50151291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459076-C-T

50151366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459147-T-C

http://identifiers.org/hco/7/GRCh38#50151419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11459199-C-A

50151419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459199-C-G

http://identifiers.org/hco/7/GRCh38#50151530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11459310-C-A

50151530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: missense variant
orthologous variants: 11459310-C-T

50151565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11459345-T-G

http://identifiers.org/hco/7/GRCh38#50151610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11459390-C-A

50151733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459506-G-A

50151963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459710-T-C

50152049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11459792-T-C

50152662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11460697-C-T

50154613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461296-C-T

50154702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461378-G-A

50154911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461601-T-A

50154992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461696-G-A

http://identifiers.org/hco/7/GRCh38#50155005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11461708-C-A

50155032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461742-G-C

50155032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461742-G-T

50155104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11461804-T-C

50155716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462384-C-T

50155817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462460-C-T

50155932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462526-G-A

50155968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462555-G-A

50156085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462671-T-C

50156133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462716-C-G

50156133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11462716-C-T

http://identifiers.org/hco/7/GRCh38#50156468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11463059-C-A

50156468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463059-C-T

50156514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463106-C-T

50156519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463111-T-C

50156524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463118-C-T

http://identifiers.org/hco/7/GRCh38#50156528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11463122-C-A

50156528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463122-C-T

50156648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463262-G-T

http://identifiers.org/hco/7/GRCh38#50156670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11463287-C-A

50156714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463333-T-A

50156714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463333-T-C

50157085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463683-G-C

50157093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463691-A-G

50157158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463756-G-A

50157162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463760-G-A

50157162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463760-G-T

50157183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463782-A-G

50157246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11463829-G-A

50157506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464052-A-G

50157630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464171-T-A

50157694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464235-C-T

50157901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464384-A-T

50157920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464392-A-G

50158000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464469-T-C

http://identifiers.org/hco/7/GRCh38#50158940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11464864-C-A

50158940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464864-C-T

50158993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: intron variant
orthologous variants: 11464924-T-C

50159046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 11464977-C-T

http://identifiers.org/hco/7/GRCh38#50159206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#11465137-C-A

50159206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22564
most severe consequence: 3 prime UTR variant
orthologous variants: 11465137-C-T