52753817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288547-T-A

52753892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288627-T-C

52753893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74288628-G-A

52754225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289084-G-T

http://identifiers.org/hco/4/GRCh38#52755147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74289915-C-A

52755147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74289915-C-T

http://identifiers.org/hco/4/GRCh38#52755245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74290016-C-A

52755245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290016-C-T

52755344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290115-C-G

http://identifiers.org/hco/4/GRCh38#52755835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74290756-A-C

52755835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290756-A-G

52755939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74290840-T-A

52758231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74291711-C-T

52759604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74292964-G-A

52759834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293179-T-C

52759999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293399-C-T

52760116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293515-A-T

52760121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293518-T-A

52760138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293535-C-T

52760232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293630-T-A

52760402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293786-T-C

52760494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74293843-C-T

52760658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294008-T-C

52760670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294022-C-T

52761084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294604-C-T

52761094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294614-A-T

52761115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74294634-A-T

52774548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74302898-G-T

52774689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303025-C-T

52774708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303044-A-G

52774740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303084-T-G

52774853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303203-A-G

http://identifiers.org/hco/4/GRCh38#52774940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74303282-A-C

52774941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303283-T-C

52775883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74303578-T-G

52775955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304162-C-T

52776017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304222-A-G

52776047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304258-G-C

52776601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74304547-A-G

52777643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305492-T-C

52777830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305667-G-T

52777831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74305668-C-T

52780537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306014-A-T

52780633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306111-C-T

52780834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306493-C-G

52780986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74306646-A-G

http://identifiers.org/hco/4/GRCh38#52781000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74306661-C-A

52781215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307167-T-C

52781215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307167-T-G

52781276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307223-G-A

52781276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307223-G-T

52781295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307231-C-T

52781335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307272-C-T

52781352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307289-A-G

52781569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307487-T-C

http://identifiers.org/hco/4/GRCh38#52781618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74307536-A-C

52782060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307700-C-T

52782140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307780-A-G

52782155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307795-A-T

52782159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74307799-T-C

http://identifiers.org/hco/4/GRCh38#52782414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74308116-C-A

52782484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308186-C-T

52782488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308192-T-C

52782523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308226-A-G

52782569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308265-T-C

52782602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308298-T-C

http://identifiers.org/hco/4/GRCh38#52782769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74308462-C-A

52782821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308511-T-A

52782825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74308515-C-T

http://identifiers.org/hco/4/GRCh38#52782972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74308644-A-C

http://identifiers.org/hco/4/GRCh38#52788396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74311007-C-A

52788467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74311086-C-T

52790587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313460-T-A

52790716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313582-A-G

52790721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313587-A-G

52790730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313596-G-A

http://identifiers.org/hco/4/GRCh38#52790820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74313669-A-C

52790820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313669-A-G

http://identifiers.org/hco/4/GRCh38#52790821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74313670-A-C

http://identifiers.org/hco/4/GRCh38#52790825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74313674-C-A

52790825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313674-C-T

52790891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313734-G-A

52790912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313753-G-A

52790939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313778-T-C

http://identifiers.org/hco/4/GRCh38#52791103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74313982-C-A

52791103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313982-C-T

52791109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313988-G-A

52791109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74313988-G-T

52791147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314014-C-G

52791285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314141-C-T

52796791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314333-G-A

52796822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314364-C-T

52796962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314498-C-G

52796962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314498-C-T

52796986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74314555-G-A

http://identifiers.org/hco/4/GRCh38#52797023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74314600-A-C

52822641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74320022-C-T

52822919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74320316-C-T

52823205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74320622-G-A

52823455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74320866-C-T

52823498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74320938-A-T

52823578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74321009-C-G

52824118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74321470-G-A

52825094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74322488-A-G

52825438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74322792-G-A

http://identifiers.org/hco/4/GRCh38#52825520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74322880-C-A

52825544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74322904-G-T

52825551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74322911-C-T

52825750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74323051-A-G

52826299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74323447-C-T

http://identifiers.org/hco/4/GRCh38#52826357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74323501-C-A

52826708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74323805-T-C

52826765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74323850-C-G

http://identifiers.org/hco/4/GRCh38#52829416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74324463-C-A

52829786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74324794-A-G

52829786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74324794-A-T

52829857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74324861-T-A

52829857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74324861-T-C

52829942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74324947-T-C

http://identifiers.org/hco/4/GRCh38#52830113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74325117-C-A

http://identifiers.org/hco/4/GRCh38#52830436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74325407-C-A

52830697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74325685-C-T

http://identifiers.org/hco/4/GRCh38#52830760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74325747-A-C

52831342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326106-C-T

52831613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326359-A-G

52831738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326456-A-G

52831807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326531-T-C

52831831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326555-C-T

52832029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326709-G-C

52832164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326828-C-G

52832298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326925-C-T

52832313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74326937-C-T

52832485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74327233-T-C

52832550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74327387-G-A

http://identifiers.org/hco/4/GRCh38#52832642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74327467-A-C

http://identifiers.org/hco/4/GRCh38#52832909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74327732-C-A

52832909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74327732-C-T

52833613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328099-A-G

52833727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328190-G-A

52833844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328452-C-T

52834120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328698-A-G

52834131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328710-A-G

52834143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328722-T-G

52834148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328727-G-T

52834187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74328765-T-G

52834619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74329223-T-C

http://identifiers.org/hco/4/GRCh38#52834748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74329355-A-C

52834748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74329355-A-T

52836502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330024-T-C

52836632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330138-G-C

52836661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330175-C-G

52836661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330175-C-T

52836698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330216-A-T

52836703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330221-C-T

52837176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330681-C-T

52837504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330952-G-A

52837508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330956-G-A

52837523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330977-G-A

52837523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74330977-G-T

52837860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74332544-C-T

52837973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74332660-T-C

52838366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74332952-C-T

http://identifiers.org/hco/4/GRCh38#52838480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74333076-A-C

52838623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74333194-C-T

52838630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74333201-T-A

52838816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74333363-G-C

52839308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74334072-G-A

52839411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74334175-C-T

52839568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74334331-A-G

52839616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74334372-T-C

52839911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74334635-C-T

52840877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74335379-G-T

52840998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335503-A-T

52841003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335508-A-T

52841078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335572-G-A

52841174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335662-C-T

52841208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335708-G-T

http://identifiers.org/hco/4/GRCh38#52841294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74335794-C-A

52841294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335794-C-T

52841438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74335923-A-T

52841772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74336238-C-T

52841782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74336248-C-G

http://identifiers.org/hco/4/GRCh38#52841874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74336353-C-A

52842057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74336541-C-T

52842114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74336599-T-G

52842368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74336842-C-T

52842609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74337387-G-C

52843107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74338008-G-A

52845938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74339532-G-A

52846068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74339651-A-G

52846224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74339784-A-G

http://identifiers.org/hco/4/GRCh38#52846244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74339804-A-C

52846414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340155-G-T

52846431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340184-G-T

52846662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340456-T-A

52846770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340570-T-C

52846781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340582-G-A

52846925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340700-T-C

52846970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340744-C-T

52847132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340911-A-G

52847146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74340925-A-G

http://identifiers.org/hco/4/GRCh38#52847310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74341057-C-A

52847532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341284-T-C

52847613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341377-T-A

52847827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341575-T-C

52848030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341722-G-T

52848063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341752-A-G

52848210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341896-T-C

52848225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74341917-G-A

52848587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74342271-C-T

http://identifiers.org/hco/4/GRCh38#52849223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74342997-C-A

52849585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74343544-A-G

52849946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74343949-G-C

52849970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74343973-G-A

52849970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74343973-G-C

52850038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74344041-T-C

52850391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74344545-C-G

52850396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74344550-C-T

52850485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74344634-G-A

52850985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345455-T-A

52850987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345457-T-C

52851134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345545-C-T

52851533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345739-A-G

52851557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345763-C-T

52851604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345806-C-T

52851667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345877-C-T

52851695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345892-A-G

52851733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345924-C-T

52851753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74345956-A-G

52852007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346208-C-T

52852070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346245-C-T

52852077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346252-C-G

52852077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346252-C-T

52852208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346365-A-G

52852237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346393-C-T

52852305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346439-C-T

52852346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346478-A-G

52852525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74346673-A-G

52853088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74347483-A-G

52853144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74347539-T-A

52853144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74347539-T-C

http://identifiers.org/hco/4/GRCh38#52853353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74348723-A-C

http://identifiers.org/hco/4/GRCh38#52853606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74348962-A-C

52853650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349003-T-G

52853722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349081-T-C

52854192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349236-G-A

52854254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349296-T-C

52854394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349400-C-T

52854531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349532-G-A

52854820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349808-T-C

52854915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74349909-T-C

52855017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74350019-C-T

52855207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74350219-C-T

52855357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74350327-G-A

52855841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74350774-A-G

52855936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74350872-C-T

52855967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74350910-C-T

52856173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351096-G-C

52858688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351705-T-C

http://identifiers.org/hco/4/GRCh38#52858849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74351879-C-A

52858849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351879-C-T

52858850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351880-T-G

52858934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351941-C-G

52858934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351941-C-T

52858937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74351944-C-T

52859326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352315-T-C

52859363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352354-G-A

52859363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352354-G-C

52859365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352364-A-G

52859377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352376-C-T

52859408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352407-A-G

52859505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352521-T-A

52859551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74352567-C-T

http://identifiers.org/hco/4/GRCh38#52859558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74352574-C-A

52859776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74353241-T-C

52859938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74353390-G-A

52859949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74353401-T-C

52859975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74353427-G-C

52860353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74353860-T-C

52860476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74354084-G-A

52861038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74354642-G-A

52861047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74354651-C-T

52861117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74354712-G-A

52861251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354836-G-A

52861254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354839-G-C

52861335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354851-T-C

52861432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354933-G-A

52861444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354940-G-C

52861470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354968-C-G

52861470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354968-C-T

52861479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74354977-T-C

52861581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74355082-C-T

52862014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74355607-G-T

52862138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74355770-C-G

http://identifiers.org/hco/4/GRCh38#52862140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74355772-C-A

52862140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74355772-C-G

52862140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74355772-C-T

http://identifiers.org/hco/4/GRCh38#52862182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74355815-C-A

52862182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355815-C-G

52862182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355815-C-T

52862190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74355823-T-C

52862263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355894-G-A

52862263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355894-G-C

52862263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355894-G-T

http://identifiers.org/hco/4/GRCh38#52862265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74355896-A-C

52862265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355896-A-G

52862265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355896-A-T

52862287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74355917-G-A

52862287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74355917-G-T

http://identifiers.org/hco/4/GRCh38#52862306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74355933-C-A

52862306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355933-C-G

52862306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355933-C-T

52862318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355944-G-C

http://identifiers.org/hco/4/GRCh38#52862326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74355952-C-A

52862326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355952-C-G

52862326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355952-C-T

52862345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355969-G-A

52862345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355969-G-T

52862355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355979-G-A

52862355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74355979-G-T

http://identifiers.org/hco/4/GRCh38#52862483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74356085-C-A

52862483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74356085-C-T

52862549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74356154-C-T

52862555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74356160-G-A

52862555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74356160-G-C

52862555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74356160-G-T

52862694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356305-T-C

52862708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356318-G-A

52862708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356318-G-T

http://identifiers.org/hco/4/GRCh38#52862709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74356319-C-A

52862709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356319-C-G

52862709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356319-C-T

http://identifiers.org/hco/4/GRCh38#52862728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74356327-C-A

52862728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356327-C-T

52862781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356356-C-T

52862879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356420-C-T

52862976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356507-T-A

52863034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74356565-G-A

52863336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74356832-C-T

52863469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74356957-T-A

52863469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74356957-T-C

52863469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74356957-T-G

http://identifiers.org/hco/4/GRCh38#52863470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74356958-C-A

52863477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74356964-G-A

http://identifiers.org/hco/4/GRCh38#52863478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74356965-C-A

52863478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74356965-C-T

http://identifiers.org/hco/4/GRCh38#52863515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74357002-C-A

52863515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74357002-C-T

http://identifiers.org/hco/4/GRCh38#52863582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74357069-C-A

52863582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74357069-C-T

http://identifiers.org/hco/4/GRCh38#52863689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74357192-C-A

http://identifiers.org/hco/4/GRCh38#52864003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74357433-C-A

52864043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74357473-T-A

52864084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74357513-G-T

http://identifiers.org/hco/4/GRCh38#52864176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74357592-A-C

52864376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74357805-G-A

52864376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74357805-G-T

52864435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74357885-G-A

52864435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74357885-G-T

52864564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358012-T-C

52864564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358012-T-G

52864596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358045-G-T

52864762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358200-T-G

http://identifiers.org/hco/4/GRCh38#52864808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74358245-A-C

http://identifiers.org/hco/4/GRCh38#52864880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74358306-C-A

52865086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358513-C-T

52865087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358514-G-A

52865087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358514-G-T

52865124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358551-T-G

52865289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358721-T-C

52865301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74358737-C-T

52865436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74358871-T-C

52865463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74358898-C-T

52865541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74358976-G-C

52865691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359126-C-G

52865691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359126-C-T

52865730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359165-A-G

http://identifiers.org/hco/4/GRCh38#52865796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74359231-C-A

52865796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359231-C-T

52866173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359534-C-T

52866247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359557-T-C

52866248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359558-T-C

52866249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359559-C-G

52866396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359683-T-C

52866436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359722-G-T

52866519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359814-G-T

52866547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359842-T-A

52866557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74359852-G-T

http://identifiers.org/hco/4/GRCh38#52866770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74360071-C-A

52866770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27195
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 74360071-C-T