http://identifiers.org/hco/2/GRCh38#96642833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36411368-C-A

96642833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36411368-C-G

96642833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36411368-C-T

http://identifiers.org/hco/2/GRCh38#96642971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36411482-C-A

96642971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36411482-C-T

http://identifiers.org/hco/2/GRCh38#96643019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36411521-A-C

96643019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36411521-A-G

96643019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36411521-A-T

http://identifiers.org/hco/2/GRCh38#96646297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36412663-C-A

96646297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36412663-C-G

96646297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36412663-C-T

http://identifiers.org/hco/2/GRCh38#96646314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36412676-A-C

96646314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36412676-A-G

96646314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36412676-A-T

96646353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36412719-G-A

96646437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36412803-A-G

http://identifiers.org/hco/2/GRCh38#96646491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36412859-C-A

96646491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36412859-C-T

96646666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413005-C-T

96646741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413084-G-A

96646897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413266-G-C

96647014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413368-G-C

96647014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413368-G-T

96647024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413377-G-T

96647025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413378-G-A

96647054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413587-C-G

96647054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413587-C-T

96647135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36413668-G-A

96647190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413724-T-C

http://identifiers.org/hco/2/GRCh38#96647205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36413739-C-A

96647205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413739-C-T

http://identifiers.org/hco/2/GRCh38#96647241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36413765-C-A

96647241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413765-C-G

96647241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413765-C-T

96647244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413768-A-G

96647247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413771-T-C

96647259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413783-A-T

http://identifiers.org/hco/2/GRCh38#96647266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36413790-C-A

96647266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413790-C-T

96647336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413851-G-A

96647489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36413995-C-G

http://identifiers.org/hco/2/GRCh38#96647569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36414052-A-C

96647738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414212-C-T

http://identifiers.org/hco/2/GRCh38#96647740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36414214-C-A

96647740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414214-C-G

96647740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414214-C-T

http://identifiers.org/hco/2/GRCh38#96647756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36414230-C-A

96647756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414230-C-T

http://identifiers.org/hco/2/GRCh38#96647762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36414236-C-A

96647762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414236-C-G

96647762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414236-C-T

96647774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36414249-C-G

96647811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36414286-A-G

96647836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36414311-C-G

96647909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414384-C-T

96647926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414393-G-A

96647944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414411-G-T

96647949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414436-G-A

96647949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414436-G-C

96647949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414436-G-T

96648082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414538-G-A

96648572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414898-G-A

96648572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414898-G-T

96648593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414923-A-G

96648611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36414941-G-A

96648949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36415161-A-G

96649157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36415335-G-C

96649176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36415354-C-T

96649584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36415772-C-G

96649584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36415772-C-T

96649649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36415836-C-G

96649649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36415836-C-T

96649686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36415873-T-C

96649946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36416724-G-A

96649969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36416747-G-A

96649982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36416762-G-T

96649985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36416765-C-T

http://identifiers.org/hco/2/GRCh38#96650176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36416932-C-A

96650176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36416932-C-G

96650176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36416932-C-T

96651831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36417399-A-G

96651984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36417560-A-G

96652058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417635-A-G

96652080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417657-G-A

96652080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417657-G-T

96652150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417719-T-A

96652174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417755-A-G

96652253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417816-T-C

http://identifiers.org/hco/2/GRCh38#96652256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36417819-C-A

96652256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417819-C-G

96652257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417820-A-G

96652367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36417919-C-T

96652513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418004-A-G

96652583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418060-A-G

96652645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418117-G-A

96652645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418117-G-T

96652705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418160-T-C

96652717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418172-A-G

96652725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418180-T-C

96652725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418180-T-G

96652737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418192-G-T

96652740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418195-G-T

96652742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418197-G-A

96652742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418197-G-T

http://identifiers.org/hco/2/GRCh38#96652789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36418228-C-A

96652859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418297-G-A

96652868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418306-G-A

96652868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418306-G-T

http://identifiers.org/hco/2/GRCh38#96652876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36418314-C-A

96652932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418363-A-G

96653588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418507-G-A

96653588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418507-G-C

96653588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418507-G-T

96653624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418543-A-G

96653732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418651-T-C

96653732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418651-T-G

96653733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418652-G-A

http://identifiers.org/hco/2/GRCh38#96653775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36418695-C-A

96653775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418695-C-T

96653796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418707-G-T

96653858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418771-T-C

http://identifiers.org/hco/2/GRCh38#96653906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36418822-C-A

96653906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418822-C-T

96653909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36418826-G-T

http://identifiers.org/hco/2/GRCh38#96654225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36419110-C-A

96654225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36419110-C-G

96654225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36419110-C-T

96654258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36419144-T-A

http://identifiers.org/hco/2/GRCh38#96654378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36419379-C-A

96654378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36419379-C-T

96654442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36419441-G-T

96655101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36419704-C-T

96660483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36422125-G-A

96660483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36422125-G-T

96660512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36422162-T-C

96660703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36422330-T-C

96660779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36422381-C-G

96660839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36422420-C-T

http://identifiers.org/hco/2/GRCh38#96661174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36423999-C-A

96661174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36423999-C-T

http://identifiers.org/hco/2/GRCh38#96661200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36424025-C-A

96661200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424025-C-T

96661211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424036-G-T

http://identifiers.org/hco/2/GRCh38#96661212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36424037-C-A

96661212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424037-C-T

96661227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424053-C-T

http://identifiers.org/hco/2/GRCh38#96661245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36424070-C-A

96661245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424070-C-T

96661445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424287-G-C

96661467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424318-T-A

96661467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424318-T-G

96661489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424340-G-T

96661514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424365-A-G

96661564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424409-C-G

http://identifiers.org/hco/2/GRCh38#96661726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36424574-C-A

96661726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense variant
orthologous variants: 36424574-C-T

96661810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424662-G-A

http://identifiers.org/hco/2/GRCh38#96662040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36424912-C-A

96662040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36424912-C-G

96662122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36425067-T-C

96662122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36425067-T-G

http://identifiers.org/hco/2/GRCh38#96662168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36425112-C-A

96662324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36425284-G-A

96662324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36425284-G-T

96663315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426148-G-A

96663315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426148-G-C

96663315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426148-G-T

96663354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426188-A-G

96663462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 36426285-A-G

http://identifiers.org/hco/2/GRCh38#96663471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36426294-C-A

96663471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant
orthologous variants: 36426294-C-G

96663538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426361-C-G

96663578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426397-G-A

http://identifiers.org/hco/2/GRCh38#96663632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36426451-C-A

96663632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426451-C-G

96663647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426467-A-G

96663647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36426467-A-T

http://identifiers.org/hco/2/GRCh38#96668662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36427585-C-A

96668679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36427596-G-C

96668735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36427652-C-T

96668946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: synonymous variant
orthologous variants: 36427858-G-A

96668946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: synonymous variant
orthologous variants: 36427858-G-C

96668946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: synonymous variant
orthologous variants: 36427858-G-T

96669010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron variant
orthologous variants: 36427926-G-A

96669171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428106-G-A

96669171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428106-G-T

http://identifiers.org/hco/2/GRCh38#96669186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36428122-C-A

96669186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428122-C-G

96669197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428133-C-G

96669197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428133-C-T

http://identifiers.org/hco/2/GRCh38#96669204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36428140-C-A

96669204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428140-C-T

http://identifiers.org/hco/2/GRCh38#96669216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36428152-C-A

96669216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428152-C-T

96669240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428177-T-C

96669272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428208-G-C

96669272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428208-G-T

96669279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428215-A-G

96669279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428215-A-T

96669507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428419-G-C

96669507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36428419-G-T

http://identifiers.org/hco/2/GRCh38#96670009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36429510-C-A

96670009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36429510-C-T

96670025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36429526-G-A

96670083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36429584-C-T

http://identifiers.org/hco/2/GRCh38#96670085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36429586-C-A

96670085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36429586-C-T

96670214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 36429704-A-G

96670306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36429799-A-G

96670306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36429799-A-T

http://identifiers.org/hco/2/GRCh38#96670317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36429853-C-A

96670317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36429853-C-T

http://identifiers.org/hco/2/GRCh38#96670373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36429909-C-A

96670373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36429909-C-T

96671415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430033-C-T

96671472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430091-G-A

96671755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430386-T-C

96672021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36430614-C-T

96672682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431044-G-T

96672747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431083-A-G

http://identifiers.org/hco/2/GRCh38#96672968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36431273-A-C

96672968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431273-A-G

96673053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431361-G-A

96673053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431361-G-T

96673055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431362-G-C

http://identifiers.org/hco/2/GRCh38#96673088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36431395-C-A

96673088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36431395-C-T

96673163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36431470-C-T

96673309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431650-G-T

96673334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431675-G-A

96673334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36431675-G-T

96673527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432139-C-T

96673542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432154-C-T

96673593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432216-A-G

http://identifiers.org/hco/2/GRCh38#96673629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36432252-C-A

96673629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432252-C-G

96674009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432583-G-A

96674454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36432992-C-T

96674491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36433033-T-G

96674508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36433050-G-A

96684117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36440224-T-C

96684161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36440252-G-A

http://identifiers.org/hco/2/GRCh38#96684262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36440366-C-A

96684262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36440366-C-T

96684272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36440376-A-G

http://identifiers.org/hco/2/GRCh38#96684547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36440633-C-A

96684603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36440695-G-T

96684750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36440877-T-C

96684908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441014-T-C

96685199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441498-A-G

96685199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441498-A-T

96685360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36441609-G-A

96685457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441704-G-A

96685457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441704-G-T

96685487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441744-T-C

96685492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441749-A-T

96685499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441756-G-A

96685499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441756-G-T

http://identifiers.org/hco/2/GRCh38#96685541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36441788-C-A

96685547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441794-T-C

96685612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36441887-G-A

http://identifiers.org/hco/2/GRCh38#96685639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36441937-C-A

http://identifiers.org/hco/2/GRCh38#96685689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36442020-A-C

96685736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442112-G-A

96685826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36442207-A-G

http://identifiers.org/hco/2/GRCh38#96685839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#36442219-C-A

96685873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442253-G-C

96685874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442254-G-T

96685917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36442275-C-T

http://identifiers.org/hco/2/GRCh38#96686051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36442409-C-A

http://identifiers.org/hco/2/GRCh38#96686197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36442555-C-A

96686197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 36442555-C-T

96686326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36442684-G-A

http://identifiers.org/hco/2/GRCh38#96686380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36442739-C-A

96686492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442890-G-A

96686492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442890-G-T

96686493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36442891-G-T

96687296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443293-C-G

96687575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443513-T-C

http://identifiers.org/hco/2/GRCh38#96687579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36443517-C-A

96687579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443517-C-T

96687646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443605-G-A

96687736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443697-G-A

96687755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443777-T-G

96687759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443779-C-T

96687790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443809-G-T

96687810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36443829-G-A

96687979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443991-C-T

96687981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443993-G-A

96687981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36443993-G-T

96687993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444005-T-G

96688006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444025-G-C

96688006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444025-G-T

96688019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444038-G-C

96688019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36444038-G-T

96689016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445421-G-A

96689016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445421-G-T

96689025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445430-T-C

96689028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445433-A-G

http://identifiers.org/hco/2/GRCh38#96689050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445455-C-A

96689050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445455-C-T

96689084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445486-C-T

http://identifiers.org/hco/2/GRCh38#96689159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445541-C-A

96689159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445541-C-T

96689232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36445609-A-G

http://identifiers.org/hco/2/GRCh38#96689305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445682-C-A

96689305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36445682-C-T

http://identifiers.org/hco/2/GRCh38#96689437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445804-C-A

96689437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445804-C-T

96689438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445805-G-A

http://identifiers.org/hco/2/GRCh38#96689505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445867-A-C

96689505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445867-A-G

96689505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445867-A-T

96689536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445901-A-G

96689536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445901-A-T

http://identifiers.org/hco/2/GRCh38#96689539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445904-A-C

96689539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36445904-A-G

http://identifiers.org/hco/2/GRCh38#96689575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36445947-C-A

http://identifiers.org/hco/2/GRCh38#96689638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446004-C-A

96689638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36446004-C-T

http://identifiers.org/hco/2/GRCh38#96689751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446117-C-A

96689796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446164-G-T

http://identifiers.org/hco/2/GRCh38#96689836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446203-C-A

96689847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446219-G-A

96689847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446219-G-C

96689847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446219-G-T

http://identifiers.org/hco/2/GRCh38#96689854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446226-C-A

96689854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446226-C-T

http://identifiers.org/hco/2/GRCh38#96689863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446233-C-A

96689873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446243-T-A

96689873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446243-T-C

96689877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446247-G-A

96689877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446247-G-C

96689877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446247-G-T

96689878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446248-G-A

96689878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446248-G-T

96689879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446249-G-A

96689879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446249-G-T

http://identifiers.org/hco/2/GRCh38#96689880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446251-C-A

96689880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446251-C-T

http://identifiers.org/hco/2/GRCh38#96690369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446870-C-A

96690369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446870-C-T

http://identifiers.org/hco/2/GRCh38#96690388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446876-C-A

96690388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446876-C-G

96690388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446876-C-T

96690453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36446932-G-A

http://identifiers.org/hco/2/GRCh38#96690516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36446993-C-A

96690516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36446993-C-T

96690562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36447039-G-A

96690718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36447195-C-T

96690726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36447203-G-A

http://identifiers.org/hco/2/GRCh38#96691063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36447466-C-A

96691063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447466-C-T

http://identifiers.org/hco/2/GRCh38#96691065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36447468-C-A

96691065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447468-C-T

http://identifiers.org/hco/2/GRCh38#96691068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36447471-C-A

96691168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447554-G-A

96691168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447554-G-C

96691168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447554-G-T

96691174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447560-G-A

http://identifiers.org/hco/2/GRCh38#96691417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36447821-C-A

96691417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447821-C-G

96691417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447821-C-T

96691419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447823-C-T

96691425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447837-T-A

96691501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36447913-C-G

96691525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36447937-C-T

96691549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36447961-C-T

96691654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448062-C-T

96691739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36448141-G-A

96691739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36448141-G-C

96691744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 36448146-A-G

96691788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36448185-C-T

http://identifiers.org/hco/2/GRCh38#96691792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36448189-C-A

96691871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36448266-C-G

96691871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36448266-C-T

96691983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448374-T-C

96692016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448395-G-A

96692017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448396-G-A

96692081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448438-A-G

http://identifiers.org/hco/2/GRCh38#96692099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36448456-C-A

96692099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36448456-C-T

96692504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449104-G-A

96692518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449118-G-A

96692653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449237-G-C

96693378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449814-G-A

96693378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449814-G-T

http://identifiers.org/hco/2/GRCh38#96693395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36449830-C-A

96693395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449830-C-G

96693395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449830-C-T

96693716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450149-A-G

96693719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450152-G-A

96693719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450152-G-C

http://identifiers.org/hco/2/GRCh38#96693820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36450241-C-A

http://identifiers.org/hco/2/GRCh38#96693850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36450254-C-A

96693877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450276-T-C

96693916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36450315-G-C

96693952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36450351-G-A

96693964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36450363-T-C

96694156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450498-A-G

http://identifiers.org/hco/2/GRCh38#96694228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36450522-C-A

96694228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450522-C-T

96694252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450544-T-C

96694267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450558-G-A

96694267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450558-G-T

96694288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450564-G-A

96694288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36450564-G-T

http://identifiers.org/hco/2/GRCh38#96694588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36450844-C-A

96694588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450844-C-T

96694603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450855-A-G

96694604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450856-G-A

96694604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450856-G-T

96694708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450907-G-A

96694708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450907-G-T

96694781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36450976-C-T

96694946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451096-G-A

96694946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451096-G-T

http://identifiers.org/hco/2/GRCh38#96694981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36451132-C-A

96695004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451154-T-C

96695138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36451324-T-C

96695138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36451324-T-G

http://identifiers.org/hco/2/GRCh38#96695167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36451353-A-C

96695167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36451353-A-G

96695226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451409-G-A

96695226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451409-G-T

96695303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451432-A-G

96695445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451583-G-A

96695445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451583-G-C

96695445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451583-G-T

http://identifiers.org/hco/2/GRCh38#96695468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36451609-C-A

96695468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451609-C-T

96695473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36451614-T-C

96695589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36451718-G-T

http://identifiers.org/hco/2/GRCh38#96695692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36451814-C-A

96695692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36451814-C-T

http://identifiers.org/hco/2/GRCh38#96695718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36451841-C-A

96695718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36451841-C-T

96695889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36452007-C-T

96695991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36452112-G-A

96695991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36452112-G-T

96696072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36452191-C-T

96696106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36452224-C-T

96697574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36453905-G-A

96697614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36453964-G-A

96697662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 36454016-T-C

96697662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36454016-T-G

96697725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36454082-C-G

96697725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36454082-C-T

96697819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454248-G-A

96697819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454248-G-C

http://identifiers.org/hco/2/GRCh38#96697868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36454500-C-A

96697868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454500-C-T

http://identifiers.org/hco/2/GRCh38#96697874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36454506-C-A

http://identifiers.org/hco/2/GRCh38#96698014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36454647-C-A

96698159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454794-G-A

96698159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454794-G-T

96698173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454806-G-C

http://identifiers.org/hco/2/GRCh38#96698266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36454902-C-A

96698266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36454902-C-T

96698362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455296-T-A

http://identifiers.org/hco/2/GRCh38#96698475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36455390-C-A

http://identifiers.org/hco/2/GRCh38#96698526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36455440-C-A

96698526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455440-C-T

96698559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455443-A-G

96698575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455459-T-C

96698596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455492-G-T

http://identifiers.org/hco/2/GRCh38#96698709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36455586-A-C

96698709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36455586-A-G

96698727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36455604-G-A

96698727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36455604-G-T

96698745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36455622-A-G

96698772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36455649-C-T

http://identifiers.org/hco/2/GRCh38#96698841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36455718-C-A

http://identifiers.org/hco/2/GRCh38#96698846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36455721-C-A

96698846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455721-C-G

96698846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455721-C-T

96698850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455725-C-T

http://identifiers.org/hco/2/GRCh38#96698883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36455784-C-A

96698883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455784-C-T

96698899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36455804-C-T

96699071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36455980-G-A

http://identifiers.org/hco/2/GRCh38#96699276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36456185-C-A

96699308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456205-G-A

http://identifiers.org/hco/2/GRCh38#96699358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36456250-A-C

96699468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456362-T-C

http://identifiers.org/hco/2/GRCh38#96699481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36456382-C-A

96699481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456382-C-T

96699510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456411-T-C

96699516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456417-A-G

http://identifiers.org/hco/2/GRCh38#96699520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36456421-C-A

96699520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456421-C-G

96699528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456424-G-T

http://identifiers.org/hco/2/GRCh38#96699649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36456545-A-C

96699825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456704-A-G

96700099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36456969-T-C

http://identifiers.org/hco/2/GRCh38#96700226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36457076-C-A

96700226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36457076-C-G

96700226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36457076-C-T

http://identifiers.org/hco/2/GRCh38#96700337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36457188-A-C

96700459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36457310-A-G

http://identifiers.org/hco/2/GRCh38#96700602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36457455-C-A

96700616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36457469-G-A

96700616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36457469-G-T

96700847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36457665-G-A

96701084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36457884-G-A

96701467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36458286-C-T

96701655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36458480-T-C

96701690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36458504-G-A

96702131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36458936-G-A

96702230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459000-C-G

http://identifiers.org/hco/2/GRCh38#96702257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36459011-C-A

96702257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459011-C-T

http://identifiers.org/hco/2/GRCh38#96702268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36459022-C-A

96702318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36459072-A-G

96702506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459263-G-A

96702506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459263-G-T

96702507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459264-C-T

96702548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459271-G-A

96702688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36459411-A-T

96702726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36459449-T-C

http://identifiers.org/hco/2/GRCh38#96702809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36459524-C-A

96702933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459636-G-A

96702933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36459636-G-T

96703190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36459891-G-A

96703320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36460018-C-T

http://identifiers.org/hco/2/GRCh38#96703468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36460152-C-A

96703468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36460152-C-G

96703585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36460270-G-A

96703597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36460282-G-A

96703638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36460323-G-C

96703754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36460435-G-T

http://identifiers.org/hco/2/GRCh38#96703776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36460455-C-A

96703776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36460455-C-T

http://identifiers.org/hco/2/GRCh38#96704243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36460590-C-A

96704243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36460590-C-G

96704243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36460590-C-T

96704329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36460676-A-G

96704683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36460987-A-G

96704685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36460989-G-A

96704685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36460989-G-C

http://identifiers.org/hco/2/GRCh38#96704785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#36461085-C-A

96704785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36461085-C-G

96704790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36461090-T-C

96704790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36461090-T-G

96704805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36461105-G-A

96704811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19044
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36461113-T-C