http://identifiers.org/hco/21/GRCh38#46098124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76459156-C-A

46111005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451443-G-C

46111025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451411-G-A

46111037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451399-G-A

46111044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451392-G-A

46111125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451318-T-G

46111253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451182-C-G

46111369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451125-G-A

46111369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451125-G-T

http://identifiers.org/hco/21/GRCh38#46111370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76451124-C-A

46111370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451124-C-T

46111402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451099-A-T

46111419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451082-G-A

46111419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76451082-G-T

http://identifiers.org/hco/21/GRCh38#46111435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76451065-C-A

46111490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76451009-C-T

46111644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76450858-C-G

46111644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76450858-C-T

46112347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76450399-G-A

46112533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76450213-A-G

46112621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450111-A-G

46112644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450106-G-A

46112644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450106-G-T

46112665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450085-T-A

46112665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450085-T-G

46112669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450081-T-C

46112669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76450081-T-G

http://identifiers.org/hco/21/GRCh38#46112773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76449992-C-A

46112773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449992-C-G

46112773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449992-C-T

46112781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449984-C-T

46112782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449983-A-G

46112858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449902-C-T

46112884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449865-G-A

46112884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449865-G-C

46112889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449860-A-G

46112901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449847-C-T

46112927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449824-G-T

46112929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449822-G-A

46112929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449822-G-C

46112929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449822-G-T

46112937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449812-G-A

46112937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449812-G-T

46112938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449811-G-A

46112938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76449811-G-T

46112955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76449789-T-C

46113025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76449712-G-A

46113025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76449712-G-T

http://identifiers.org/hco/21/GRCh38#46113072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76449670-A-C

46113072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76449670-A-G

http://identifiers.org/hco/21/GRCh38#46113085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76449659-C-A

46113085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76449659-C-T

46113086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76449658-G-A

46114078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449082-G-A

46114078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76449082-G-T

http://identifiers.org/hco/21/GRCh38#46114079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76449081-A-C

46114592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448873-A-G

46114658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448798-C-T

46114704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448753-T-A

46114704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448753-T-C

46114918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448600-G-A

46115105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448486-T-C

46115105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448486-T-G

46115347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448306-C-T

46115583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448091-G-A

46115652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76448031-T-G

http://identifiers.org/hco/21/GRCh38#46115748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76447937-C-A

46115748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447937-C-T

46115756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447929-G-A

46115756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447929-G-T

46115812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447877-T-G

46115946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447729-C-G

46115956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447719-C-T

http://identifiers.org/hco/21/GRCh38#46116187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76447487-A-C

http://identifiers.org/hco/21/GRCh38#46116247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76447437-A-C

http://identifiers.org/hco/21/GRCh38#46116263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76447421-A-C

46116283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447400-A-G

46116532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447141-G-T

46116556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76447117-T-C

46116858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76446821-G-A

46116858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76446821-G-C

46116858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76446821-G-T

http://identifiers.org/hco/21/GRCh38#46116920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76446787-C-A

46116920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76446787-C-T

46116921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76446786-A-G

46116921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76446786-A-T

46117588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76446344-A-G

46117588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76446344-A-T

http://identifiers.org/hco/21/GRCh38#46117638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76446296-C-A

46117638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76446296-C-G

46117638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76446296-C-T

46117657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76446273-G-A

46117657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76446273-G-T

http://identifiers.org/hco/21/GRCh38#46117877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76446051-C-A

46117877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76446051-C-T

46117954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445975-G-A

46117954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445975-G-T

http://identifiers.org/hco/21/GRCh38#46117963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76445959-C-A

46117963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445959-C-T

http://identifiers.org/hco/21/GRCh38#46118000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76445916-C-A

46118000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445916-C-T

46118069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445849-G-A

46118069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445849-G-T

http://identifiers.org/hco/21/GRCh38#46118129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76445770-C-A

46118129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445770-C-T

46118158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445725-G-A

46118284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445630-C-T

http://identifiers.org/hco/21/GRCh38#46118285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76445629-C-A

46118291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445623-G-A

46118291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445623-G-T

46118604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445424-A-G

46118615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 76445413-G-A

46118615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 76445413-G-C

http://identifiers.org/hco/21/GRCh38#46118726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76445328-C-A

46118740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445314-A-G

46118822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445262-G-C

http://identifiers.org/hco/21/GRCh38#46118977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76445218-C-A

46118977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76445218-C-T

46119365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444895-G-A

46119689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444663-T-C

46119689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444663-T-G

46119706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444646-G-A

46119706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444646-G-C

46119828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76444562-G-A

46119828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76444562-G-T

46119864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444526-T-C

46119864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444526-T-G

http://identifiers.org/hco/21/GRCh38#46119916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76444476-C-A

http://identifiers.org/hco/21/GRCh38#46119953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76444441-A-C

46119953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444441-A-G

http://identifiers.org/hco/21/GRCh38#46120062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76444309-C-A

46120413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444097-C-T

http://identifiers.org/hco/21/GRCh38#46120454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76444059-C-A

46120454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444059-C-T

46120465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444046-G-A

46120465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444046-G-C

46120465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76444046-G-T

http://identifiers.org/hco/21/GRCh38#46120536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76443980-C-A

46120536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76443980-C-T

46120608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443922-G-A

46120608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443922-G-T

46120649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443887-T-G

46120707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443881-G-A

46120707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443881-G-T

46120720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443868-A-G

46120952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443735-C-G

46120952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443735-C-T

46121000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443690-T-G

http://identifiers.org/hco/21/GRCh38#46121293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76443290-C-A

46121308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443275-C-T

http://identifiers.org/hco/21/GRCh38#46121311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76443272-C-A

46121311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443272-C-G

46121311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443272-C-T

46121452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443094-G-A

46121452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443094-G-T

46121513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443032-G-A

46121538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76443007-T-C

46121562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76442983-C-G

46121562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76442983-C-T

46121577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76442968-G-A

46121630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442917-T-C

46121663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442893-G-A

46121696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442848-G-A

46121715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442831-G-T

46121818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442706-C-G

46122008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442533-C-T

46122047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442504-A-G

46122068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442493-G-A

46122068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442493-G-C

http://identifiers.org/hco/21/GRCh38#46122082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76442483-C-A

46122213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442373-G-A

46122272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442342-G-A

46122273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442341-T-G

46122285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442328-G-A

http://identifiers.org/hco/21/GRCh38#46122303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76442308-C-A

46122303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442308-C-G

46122303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442308-C-T

46122313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442292-C-T

http://identifiers.org/hco/21/GRCh38#46122381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#76442189-C-A

46122381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, undefined
orthologous variants: 76442189-C-T

46122399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442141-G-A

46122407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76442133-G-A

46122511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76442024-C-G

46122548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441987-G-A

46122548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441987-G-C

46122555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441980-G-A

46122557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441978-G-A

http://identifiers.org/hco/21/GRCh38#46122599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76441946-A-C

46122599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441946-A-G

http://identifiers.org/hco/21/GRCh38#46122629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76441927-C-A

46122629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441927-C-G

46122629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441927-C-T

46122659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441902-G-A

46122659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441902-G-T

46122733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441842-A-G

46122733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441842-A-T

46122826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441709-G-A

46122826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441709-G-C

http://identifiers.org/hco/21/GRCh38#46122908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76441635-C-A

46122908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76441635-C-G

46122908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76441635-C-T

46122923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76441620-G-A

46122923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76441620-G-C

46123011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441547-T-C

46123026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441537-G-A

46123090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441491-C-T

http://identifiers.org/hco/21/GRCh38#46123109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76441471-A-C

46124307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441252-G-A

46124365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441202-C-T

46124401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441161-G-C

46124439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441135-G-A

46124461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441113-C-T

46124477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441097-C-G

46124477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441097-C-T

46124509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441066-A-G

46124596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76441006-G-A

http://identifiers.org/hco/21/GRCh38#46124690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440915-C-A

http://identifiers.org/hco/21/GRCh38#46124799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440804-C-A

46124799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440804-C-G

46124799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440804-C-T

46124843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440752-A-G

46124874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440727-T-C

http://identifiers.org/hco/21/GRCh38#46124943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440658-C-A

46124943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440658-C-G

46124943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440658-C-T

46125022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440576-A-G

46125103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440407-G-A

46125114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440394-G-A

46125114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440394-G-T

46125126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440382-G-A

46125126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440382-G-T

46125170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440319-G-A

46125170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440319-G-T

46125195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440302-G-C

46125214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440283-A-G

46125367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440140-T-A

46125367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440140-T-C

46125367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440140-T-G

http://identifiers.org/hco/21/GRCh38#46125386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440131-C-A

46125386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440131-C-T

46125407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76440109-G-A

46125416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 76440100-G-A

46125416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 76440100-G-T

http://identifiers.org/hco/21/GRCh38#46125423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440093-A-C

46125423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant
orthologous variants: 76440093-A-G

46125423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant
orthologous variants: 76440093-A-T

http://identifiers.org/hco/21/GRCh38#46125444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440067-A-C

46125444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant
orthologous variants: 76440067-A-G

46125444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant
orthologous variants: 76440067-A-T

46125451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76440055-T-C

46125451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76440055-T-G

http://identifiers.org/hco/21/GRCh38#46125458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76440047-C-A

46125458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 76440047-C-T

46125581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: synonymous variant
orthologous variants: 76439924-C-T

http://identifiers.org/hco/21/GRCh38#46125665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76439876-C-A

46125665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439876-C-T

46125666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439875-G-A

46125666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439875-G-T

46125681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439859-A-G

46125745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439809-C-T

46125766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439772-T-G

46125773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439765-T-A

46125773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439765-T-C

http://identifiers.org/hco/21/GRCh38#46125922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76439609-A-C

46126084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76439447-A-G

46126221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: synonymous variant
orthologous variants: 76439310-G-A

http://identifiers.org/hco/21/GRCh38#46126373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76439278-C-A

46126373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439278-C-T

46126464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76439232-C-T

http://identifiers.org/hco/21/GRCh38#46126585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76439118-A-C

46126744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438972-G-A

46126832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438831-T-C

46126868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438721-C-T

46126953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438625-C-G

46127169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438428-T-A

46127287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438305-T-C

46127309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438284-C-G

46127404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438205-G-A

46127418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438191-G-A

46127418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76438191-G-C

46128981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435942-C-T

http://identifiers.org/hco/21/GRCh38#46129020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76435907-C-A

46129020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435907-C-T

46129021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435906-C-G

46129021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435906-C-T

http://identifiers.org/hco/21/GRCh38#46129040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76435886-C-A

46129040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435886-C-G

46129040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435886-C-T

http://identifiers.org/hco/21/GRCh38#46129093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76435831-A-C

46129109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435811-T-C

46129305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 76435616-C-T

46129608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435254-G-A

46129608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435254-G-T

http://identifiers.org/hco/21/GRCh38#46129654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76435152-A-C

46129654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435152-A-G

46129672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435088-T-A

46129672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435088-T-G

46129678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435082-G-T

46129687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435073-G-A

46129687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76435073-G-T

46129906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434823-T-A

46129906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434823-T-C

46129906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434823-T-G

http://identifiers.org/hco/21/GRCh38#46129909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76434820-C-A

46129909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434820-C-G

46129909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434820-C-T

46129933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434787-G-T

46129941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434779-T-C

46129941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434779-T-G

46129956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434749-G-A

46129956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434749-G-T

46130194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434423-C-T

46130271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434364-G-T

46130272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434363-C-T

46130352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434279-G-A

46130362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434269-C-G

46130362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434269-C-T

46130417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434193-T-C

46130503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434099-C-T

46130573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434027-C-G

46130573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434027-C-T

46130574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76434026-C-T

46130655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433944-G-A

46130717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433882-G-A

46130758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433842-C-T

46130767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433833-A-G

46130854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433776-A-G

46130877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433752-T-C

46131072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433468-C-G

46131160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433414-C-G

46131184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433390-G-A

46131276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433302-G-T

46131315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433265-G-A

46131315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76433265-G-C

46131600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432989-T-G

46131790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432818-A-G

46131793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432815-G-C

46131806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432798-G-C

46131806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432798-G-T

46131894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432706-G-A

46131894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432706-G-T

http://identifiers.org/hco/21/GRCh38#46131913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76432687-C-A

46131913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: intron variant
orthologous variants: 76432687-C-T

46132025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432572-G-C

46132247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432350-G-A

46132247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432350-G-T

46132259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432338-C-T

46132286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432311-C-G

http://identifiers.org/hco/21/GRCh38#46132406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#76432191-A-C

46132406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432191-A-G

46132415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432182-G-A

46132415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432182-G-T

46132421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432176-G-A

46132421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432176-G-C

46132427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432170-G-A

46132427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432170-G-T

46132472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432125-G-A

46132472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2212
most severe consequence: missense variant
orthologous variants: 76432125-G-T