50182357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395002-G-A

50182357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395002-G-C

50182357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395002-G-T

50182385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395029-T-C

50182386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395030-G-A

50182386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395030-G-T

50182394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395038-T-C

http://identifiers.org/hco/15/GRCh38#50182400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#126395044-C-A

50182400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 126395044-C-T

50182555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126395202-T-G

50182566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126395213-G-A

50182566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126395213-G-C

50182566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126395213-G-T

50182580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 126395227-G-A

50182610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 126395257-G-A

50182610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 126395257-G-C

50182841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: missense variant
orthologous variants: 126395488-C-G

50182898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: synonymous variant
orthologous variants: 126395545-G-T

http://identifiers.org/hco/15/GRCh38#50182947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126395599-C-A

50182947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126395599-C-T

50182949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126395601-G-T

50182965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126395616-G-C

50182965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126395616-G-T

50183097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126395851-G-C

50183116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126395896-G-A

50183861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396333-A-G

50183892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396364-A-G

50184453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396592-G-A

50184471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396610-C-T

50184494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396633-T-G

50184891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396717-G-C

50184942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396750-G-A

50184944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396752-T-A

50184964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396770-T-A

50185086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396892-C-T

50185183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126396994-T-C

50185229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126397328-A-G

50185311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126397410-G-A

50187129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126400365-T-A

50187396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126400622-T-C

50196098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402589-A-G

http://identifiers.org/hco/15/GRCh38#50196143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126402634-C-A

50196143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402634-C-T

50196145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402636-T-G

50196297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402786-G-A

50196340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402822-T-A

50197024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402866-C-T

50197118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126402951-C-T

50197377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126403340-G-A

50197424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126403385-T-A

http://identifiers.org/hco/15/GRCh38#50197648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126403605-A-C

50198007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126403967-T-A

50198007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126403967-T-C

50198091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126404050-A-T

50198201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126404123-T-C

50198342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126404226-G-A

50198342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126404226-G-T

50198405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126404283-T-C

50198438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 126404299-A-G

50199051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126404832-G-T

50199199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126404969-T-A

50199971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405208-T-G

50200557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405566-A-G

50200632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405615-C-T

50200751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405710-A-T

50200840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405793-T-A

50200840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405793-T-C

50200840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126405793-T-G

50201941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406202-G-A

50201954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406215-C-T

50202053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406310-G-T

50202125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406352-C-T

50202524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, missense_variant
orthologous variants: 126406635-A-G

50202581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126406692-T-C

http://identifiers.org/hco/15/GRCh38#50202611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126406722-A-C

50202611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126406722-A-G

50202638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126406749-T-C

50202638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, missense_variant
orthologous variants: 126406749-T-G

50202686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406798-T-C

http://identifiers.org/hco/15/GRCh38#50202705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126406817-C-A

50202705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406817-C-T

50202759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406864-G-T

50202781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406886-A-G

50202781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406886-A-T

50202895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126406980-T-G

50202945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407043-C-T

50203261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407280-T-C

50203264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407283-A-G

50203294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407292-C-T

http://identifiers.org/hco/15/GRCh38#50203345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126407342-A-C

50203345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407342-A-G

50203461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407429-T-C

50203648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126407619-A-G

50204975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126409441-T-C

50205088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126409569-A-G

50205088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126409569-A-T

50205235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 126409663-G-A

50205288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: missense variant
orthologous variants: 126409716-T-A

50205288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: synonymous variant
orthologous variants: 126409716-T-C

50205445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126409870-C-G

http://identifiers.org/hco/15/GRCh38#50205514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126409941-C-A

50205514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126409941-C-G

50205515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126409942-C-T

http://identifiers.org/hco/15/GRCh38#50205531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126409958-A-C

50205540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126409967-G-C

50205588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126410015-G-T

50205821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126410176-T-C

50206388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126410722-C-T

50206499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126410850-G-A

50206561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126410911-C-T

50206915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126411259-G-T

50209208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126412152-C-T

50209376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126412282-G-A

50209381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126412287-C-T

50209404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126412310-G-A

50209454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126412359-G-C

50209776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126412581-C-T

50219637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126413689-G-A

50219745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126413808-A-G

50220499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126414560-C-T

50220575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126414625-G-A

50220582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126414626-G-C

50220637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126414683-G-A

50221476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126415186-A-G

http://identifiers.org/hco/15/GRCh38#50221499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126415199-A-C

50221528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126415224-G-A

50221734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126415648-C-T

50221787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126415691-C-T

50221856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126415759-A-G

50222108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126415841-C-T

http://identifiers.org/hco/15/GRCh38#50222801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126416457-C-A

50222877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416537-A-G

50222890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416550-A-G

50222893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416553-G-A

50222893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416553-G-T

50223171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416829-G-A

50223171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416829-G-C

50223200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416858-C-T

50223202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416860-G-A

50223223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416876-G-A

50223232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416885-T-C

50223233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416886-G-A

50223233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416886-G-T

50223269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416927-T-C

50223271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416929-G-A

50223271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416929-G-T

50223341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126416986-A-T

50223435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126417052-A-G

50224388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126417764-C-G

50224580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126417834-G-C

50224580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126417834-G-T

50225008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126418345-A-G

50225685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126419463-T-C

50225779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126419556-A-G

50225783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126419560-G-T

50225955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126419743-G-T

50226038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126419830-T-A

http://identifiers.org/hco/15/GRCh38#50226097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126419888-C-A

http://identifiers.org/hco/15/GRCh38#50226228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126420019-C-A

50226362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420136-C-T

50226370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420144-T-C

50226707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420474-G-A

50226707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420474-G-C

50226723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420498-T-C

50226789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420546-G-A

http://identifiers.org/hco/15/GRCh38#50226874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126420644-C-A

50226874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420644-C-T

50226880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420650-G-T

50226928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420701-G-A

50226938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420714-G-T

http://identifiers.org/hco/15/GRCh38#50226947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126420726-C-A

50226947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420726-C-T

50226949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420728-C-T

50226960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126420749-T-C

50226973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 126420762-G-C

http://identifiers.org/hco/15/GRCh38#50227195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126420984-C-A

50227237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126421031-T-A

50227237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126421031-T-C

50227271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126421069-T-C

50227339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126421115-T-C

50227575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126421497-G-A

50227884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126421800-G-C

50228728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422650-T-A

50228728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422650-T-C

http://identifiers.org/hco/15/GRCh38#50228801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126422735-A-C

50228801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422735-A-G

50228820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422753-G-T

50228824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422757-C-T

http://identifiers.org/hco/15/GRCh38#50228934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126422815-C-A

50228934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422815-C-T

50228963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: synonymous variant
orthologous variants: 126422844-G-A

50229048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126422929-T-G

50229157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126423011-A-G

50229190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126423044-T-A

50229190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126423044-T-C

50229383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126423217-G-C

50229559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126423397-C-T

50229561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126423399-G-T

http://identifiers.org/hco/15/GRCh38#50229622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126423435-C-A

50231755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126425981-G-A

50231873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126426094-G-A

50232084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126426277-T-C

50232202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126426385-A-G

50232298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126426467-G-A

50232621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126426752-C-T

50232632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126426763-C-T

50232989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427117-G-T

50233134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427257-T-G

http://identifiers.org/hco/15/GRCh38#50233155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126427278-C-A

50233239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427349-T-C

50233413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427536-T-A

50233413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427536-T-C

50233475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427595-C-T

50233502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427654-C-G

50233606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427754-G-A

50233654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126427782-G-A

http://identifiers.org/hco/15/GRCh38#50233795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126428101-C-A

50233795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126428101-C-G

http://identifiers.org/hco/15/GRCh38#50233813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126428119-A-C

50233825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126428131-A-G

50233897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: missense variant
orthologous variants: 126428201-A-G

50233951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: missense variant
orthologous variants: 126428255-G-A

http://identifiers.org/hco/15/GRCh38#50234056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126428347-A-C

50234056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126428347-A-G

50235141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126428955-G-T

50235163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126428980-T-C

50235477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126429233-C-T

50235487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126429243-G-A

50235594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: intron variant
orthologous variants: 126429348-A-G

http://identifiers.org/hco/15/GRCh38#50236118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126429881-A-C

50236130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126429893-A-G

http://identifiers.org/hco/15/GRCh38#50236139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#126429902-A-C

50236161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126429935-T-C

50236187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126429961-T-A

50236225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126430001-G-A

50236225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126430001-G-C

50236225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126430001-G-T

50236274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126430059-G-A

50236383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 10996
most severe consequence: 3 prime UTR variant
orthologous variants: 126430168-T-A