49532105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474562-A-T

49532196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474471-A-G

49532417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474210-G-T

49532448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474182-G-A

http://identifiers.org/hco/13/GRCh38#49532467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59474162-C-A

49532493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474133-G-T

49532528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474100-T-C

49532577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474057-G-T

http://identifiers.org/hco/13/GRCh38#49532600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59474034-C-A

49532600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474034-C-T

49532604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474030-G-A

49532612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59474024-G-T

49532654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473976-G-A

49532970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473946-G-A

http://identifiers.org/hco/13/GRCh38#49533012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59473905-C-A

49533022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473899-G-C

49533032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473889-G-T

49533088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473819-A-G

49533119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473792-G-C

49533120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473791-G-T

http://identifiers.org/hco/13/GRCh38#49533144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59473753-C-A

49533175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473722-A-T

49533289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473659-G-A

49533297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473651-T-C

49533353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473608-T-C

49533416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473537-C-T

http://identifiers.org/hco/13/GRCh38#49533424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59473529-C-A

49533702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473239-G-T

49533759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473191-T-A

49533759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473191-T-C

49533759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473191-T-G

49533873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473013-G-A

49533873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473013-G-T

49533874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59473012-T-C

49533998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59472883-A-G

49533998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59472883-A-T

49534033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59472866-T-C

49534033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59472866-T-G

49534105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59472822-C-T

49534201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59472727-G-A

49534320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472608-T-C

49534332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472596-G-T

http://identifiers.org/hco/13/GRCh38#49534357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59472571-C-A

49534442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472510-C-T

49536964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59471867-A-G

49537122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59471706-G-C

49539209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59470683-T-A

49539209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59470683-T-C

49539385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59470534-A-G

49539706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469222-G-A

49539720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469209-T-C

49539789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469144-A-G

http://identifiers.org/hco/13/GRCh38#49540051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59468921-A-C

49540051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468921-A-G

49540120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468865-C-T

49540164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468820-C-G

49540228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468753-G-A

49540273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468718-C-T

49540356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468530-C-T

49540374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468438-C-G

49540399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468388-A-G

49540447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59468348-T-C

49540724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59468112-A-G

49540740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59468096-A-T

http://identifiers.org/hco/13/GRCh38#49540796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59468053-C-A

49540796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59468053-C-T

49540799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59468050-G-T

49541007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 59467856-C-T

49541289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467683-T-C

49541546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467603-T-A

49541546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467603-T-C

49541546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467603-T-G

http://identifiers.org/hco/13/GRCh38#49541557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59467593-C-A

49541557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467593-C-G

49541557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467593-C-T

http://identifiers.org/hco/13/GRCh38#49541586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59467567-C-A

49541586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467567-C-T

49541593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467560-A-T

49541646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467510-G-A

49541646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467510-G-T

http://identifiers.org/hco/13/GRCh38#49541650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59467506-C-A

49541650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467506-C-G

49541650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467506-C-T

49541690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59467471-G-A

49542273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467237-C-T

49543659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59466433-G-A

49544559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59466007-C-T

49544593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465976-A-G

49544598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465971-G-A

49544598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465971-G-C

49544598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465971-G-T

49544622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465946-T-A

http://identifiers.org/hco/13/GRCh38#49544648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59465920-C-A

49544668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465900-A-T

http://identifiers.org/hco/13/GRCh38#49544909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59465655-A-C

49544909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465655-A-G

49544944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465624-G-A

49544944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465624-G-T

49545001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465571-A-T

49547075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59464528-G-A

49547075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59464528-G-T

49547126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59464473-A-T

49547213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59464383-G-A

49547226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59464370-T-A

49547226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59464370-T-C

http://identifiers.org/hco/13/GRCh38#49547256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59464346-A-C

http://identifiers.org/hco/13/GRCh38#49549371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59464028-A-C

http://identifiers.org/hco/13/GRCh38#49549383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59464007-C-A

49549399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463991-A-G

49549499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59463904-C-G

49549508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59463895-A-G

49549538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59463865-T-A

49549765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59463639-A-G

49549765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59463639-A-T

http://identifiers.org/hco/13/GRCh38#49549791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59463613-A-C

49549791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59463613-A-G

49549821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59463547-T-C

49549863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59463502-T-C

49549863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59463502-T-G

49549949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463413-G-A

49550288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59462810-A-G

49550346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59462751-A-T

49551208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59462331-C-T

49551212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59462327-A-G

49551220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59462319-T-C

49551272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59462274-A-G

49551290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59462259-C-T

49551312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59462236-C-T

49552012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461859-G-T

49552051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461820-A-G

49552055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461816-G-C

http://identifiers.org/hco/13/GRCh38#49552093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59461778-C-A

49552093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461778-C-T

49552111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461760-A-G

49552134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460789-G-A

49552134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460789-G-T

49552136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460787-A-G

49552292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59460633-G-T

49552305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460622-A-G

49552329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460604-G-A

49552329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460604-G-T

http://identifiers.org/hco/13/GRCh38#49552350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59460592-A-C

49552374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460571-G-A

49552374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460571-G-T

http://identifiers.org/hco/13/GRCh38#49552390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59460556-A-C

49552390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460556-A-T

http://identifiers.org/hco/13/GRCh38#49552398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59460546-C-A

49552398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460546-C-T

49552437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460522-T-C

49552437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460522-T-G

49552554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460466-A-T

49552650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460376-T-C

49552655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460371-G-T

49552672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460354-T-A

49552672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460354-T-C

http://identifiers.org/hco/13/GRCh38#49552864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59460173-A-C

49552913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460122-G-A

49552956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460083-G-C

49552968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460072-G-A

49553596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59459633-T-C

49553718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59459511-C-T

49555505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59459032-G-A

http://identifiers.org/hco/13/GRCh38#49556576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59457382-A-C

49557085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59456831-T-C

49557486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59456509-T-C

49557503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59456491-A-G

49559879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59455238-A-G

49559887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59455230-A-T

49559969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59455158-C-T

49560036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59455091-T-A

49560036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59455091-T-C

49560223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454938-G-A

49560223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454938-G-T

49560230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454929-G-A

49560230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454929-G-T

49563960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450688-T-C

49566259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448909-A-T

49566357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448784-T-C

49566477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448157-C-G

49566477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448157-C-T

49566644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59448006-C-G

49566644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59448006-C-T

49566772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59447878-G-A

49566772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59447878-G-T

49566781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447869-T-C

49566798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447854-C-T

http://identifiers.org/hco/13/GRCh38#49566857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59447791-A-C

49566862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447786-A-G

49566862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447786-A-T

49566907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447741-T-G

49566914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447734-T-C

49566917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447731-G-A

49566917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447731-G-T

49567001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447665-C-T

49567116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447574-A-G

49567134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447556-A-G

http://identifiers.org/hco/13/GRCh38#49567170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59447525-A-C

http://identifiers.org/hco/13/GRCh38#49567363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59447329-C-A

http://identifiers.org/hco/13/GRCh38#49567405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59447283-C-A

49567413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447275-G-T

49570316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444519-T-A

49570490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444356-G-C

49570607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444222-A-G

49576784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443760-T-C

49576989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443618-A-G

49577066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443564-G-A

49577143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443489-G-A

49577252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443397-G-A

49577252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443397-G-C

49577297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443347-G-A

49577594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443075-T-C

49577660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443035-G-T

49577705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442991-G-C

49577786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442935-T-C

49577881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442832-T-C

49578467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442572-A-G

49578531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442504-T-A

49578776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442272-A-G

49580014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441348-T-C

49584037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439651-C-G

49584054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439640-C-G

49584320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439416-A-G

49584403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439346-G-A

49584403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439346-G-T

49584508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439305-C-T

http://identifiers.org/hco/13/GRCh38#49584678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59439138-C-A

49584763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18243
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439061-T-C