110243988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40688641-G-A

110244199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687946-G-A

110244223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687928-A-G

110244278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687872-C-G

110244278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687872-C-T

110244325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687827-G-A

110244325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687827-G-C

110245375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687773-G-A

110245453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687694-G-C

110245576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40687113-A-G

110245811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40686845-G-T

http://identifiers.org/hco/6/GRCh38#110245813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40686843-C-A

110245813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40686843-C-T

110245832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40686813-G-A

110245832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40686813-G-T

http://identifiers.org/hco/6/GRCh38#110245895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40686751-C-A

110245933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40686729-G-A

110245933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40686729-G-T

110246001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40686659-A-T

110246003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40686657-G-A

110246030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40686630-A-G

110246058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40686602-C-T

110246331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686284-T-C

110246332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686283-A-G

110246378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686225-G-A

110246378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40686225-G-T

110246406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40685082-T-C

110246633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40685002-T-C

http://identifiers.org/hco/6/GRCh38#110246646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40684989-C-A

110246706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684933-T-C

110246769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684856-A-G

110246830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684814-C-T

110246840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684804-G-A

110246931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684730-T-A

110246931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684730-T-C

110247078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684585-G-C

110247111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40684552-T-G

110248516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40683471-G-A

http://identifiers.org/hco/6/GRCh38#110248643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40683349-C-A

110248835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40683305-C-T

110248874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40683267-A-G

110248875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40683266-G-C

110248932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40683209-T-C

110249183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40682677-C-T

110249230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40682589-A-T

110249478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40682337-A-G

110249885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681933-T-A

http://identifiers.org/hco/6/GRCh38#110249923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40681895-C-A

110250054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681766-T-C

110250121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681702-T-C

110250523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681390-T-C

110250530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681383-G-C

110250743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681188-C-T

110250846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40681094-T-G

110251156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40680792-G-A

http://identifiers.org/hco/6/GRCh38#110251300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40680671-A-C

110252807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40673886-C-T

110252837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40673822-T-C

110252972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40673691-T-C

110253042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40673644-T-G

110253085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40673597-T-G

110253123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40673564-T-G

110253508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40672935-A-G

http://identifiers.org/hco/6/GRCh38#110253750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40672757-C-A

http://identifiers.org/hco/6/GRCh38#110253793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40672722-A-C

http://identifiers.org/hco/6/GRCh38#110253795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40672720-C-A

110253795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40672720-C-T

110253869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40672650-A-G

http://identifiers.org/hco/6/GRCh38#110253920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40672605-C-A

110253964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672575-G-A

110253964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672575-G-T

110254007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672524-G-A

110254007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672524-G-C

110254007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672524-G-T

110254008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672523-A-G

110254008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672523-A-T

110254043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672485-A-G

110254082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672445-A-G

110254121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672403-T-C

110254140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672380-T-A

110254191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40672329-G-A

http://identifiers.org/hco/6/GRCh38#110254234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40672287-C-A

110254801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40671309-T-C

110254934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40671170-T-C

110254952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40671169-A-T

http://identifiers.org/hco/6/GRCh38#110255520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40670238-A-C

110255670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, undefined
orthologous variants: 40670103-T-G

110257462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40669405-T-C

110257553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40669301-T-A

110257649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40669205-G-T

110257981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668859-T-C

http://identifiers.org/hco/6/GRCh38#110258000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40668839-C-A

110258000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668839-C-T

http://identifiers.org/hco/6/GRCh38#110258278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40668292-C-A

110258278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668292-C-T

110258319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668251-C-T

110258425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668173-G-A

110258492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668104-G-T

110258529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668070-G-A

110258580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668038-G-A

110258596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668022-G-A

110258596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668022-G-T

110258607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40668012-T-C

110265175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40667674-A-T

110265281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40667517-C-G

http://identifiers.org/hco/6/GRCh38#110265399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40667350-C-A

110265399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40667350-C-T

110266585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40659975-C-T

110266630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40659933-T-A

110266671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40659892-C-T

http://identifiers.org/hco/6/GRCh38#110266672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40659891-C-A

110266816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40659568-T-C

110267101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40658405-A-T

110267411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40658125-C-G

110267416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40658120-G-A

110267456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40658079-A-T

110268543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40657776-T-C

110268546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40657758-G-T

110268605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40657690-A-G

110268879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40657430-C-T

110269125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40657160-T-C

110269126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40657159-G-A

110269408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40656603-A-T

110269679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40656143-T-G

http://identifiers.org/hco/6/GRCh38#110269865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40655959-A-C

110270578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40655300-T-A

110270590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40655288-G-C

110270745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40655137-T-C

110271934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40654538-T-C

http://identifiers.org/hco/6/GRCh38#110276067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40652199-C-A

110276067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40652199-C-T

110276499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40652093-T-C

110276638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40651973-G-C

http://identifiers.org/hco/6/GRCh38#110276647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40651964-A-C

110276731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40651883-G-A

110276809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40651845-G-C

110277006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40651696-A-G

110277083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40651620-T-C

110278386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40650395-G-A

110279163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647746-T-C

110279192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647731-G-A

http://identifiers.org/hco/6/GRCh38#110279238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40647685-A-C

110279382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647533-T-C

110279601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647303-A-G

110279633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647271-A-G

110279633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647271-A-T

110279707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647208-G-A

110279707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40647208-G-T

110280400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646754-A-G

110280417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646736-T-C

110280533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646622-T-A

110280929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646520-A-G

110281078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646384-T-A

110281216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646246-T-C

110281216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646246-T-G

110281266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40646197-G-T

110281357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: -C-T

110281864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40644890-C-T

http://identifiers.org/hco/6/GRCh38#110281890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40644864-A-C

110282138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40644698-G-T

110282748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40641618-C-T

http://identifiers.org/hco/6/GRCh38#110283201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40641154-C-A

110283201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40641154-C-G

110283268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40641137-A-G

110283389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40641028-T-C

110283476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40640933-G-A

110283611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40640805-T-A

110283690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40640726-T-C

110283764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40640649-T-C

110284966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40638929-C-T

110284998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40638897-T-C

110285241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40638655-G-C

110285860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637948-A-G

110285955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637851-C-T

110285956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637850-G-A

110285985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637825-T-C

110286171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637623-G-A

110286246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637558-G-A

110286246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637558-G-C

110286473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637230-G-A

110286477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637227-T-C

110286485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637219-G-A

110287088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40637048-T-C

110287188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40636950-A-T

110287229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40636903-A-G

110287500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40636613-G-T

110287570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40636557-C-T

110287905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40636117-C-T

http://identifiers.org/hco/6/GRCh38#110288330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40635281-C-A

110288354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40635250-G-A

110288412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40635182-T-G

110288554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40635053-C-T

http://identifiers.org/hco/6/GRCh38#110288685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40634939-C-A

110288685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634939-C-G

110288786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634850-G-A

110288788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634848-G-A

110288792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634844-C-T

110288829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634802-G-T

110288995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634635-C-T

http://identifiers.org/hco/6/GRCh38#110289048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40634583-C-A

110289085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40634543-T-C

110295382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40629319-T-C

110295625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40629099-C-T

110295715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40629006-C-T

110295809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40628912-G-A

110295809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40628912-G-T

110295901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40628848-T-C

110295951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40628798-T-C

110296347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626984-A-G

110296351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626980-C-T

110296482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626848-A-G

110296608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626722-G-C

110296739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626602-C-T

110296781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626566-G-A

110296850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626499-C-G

110297135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626290-T-G

110297234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626179-T-C

110297338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40626050-C-T

110297708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40625697-T-G

110297855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40625551-C-T

110298772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622706-T-A

110298806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622672-A-G

110298852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622624-G-A

110298852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622624-G-T

110298992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: missense variant
orthologous variants: 40622484-A-G

110298993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: missense variant
orthologous variants: 40622483-C-T

110299104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: missense variant
orthologous variants: 40622372-C-T

110299139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40622337-T-C

110299165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622313-G-A

110299165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622313-G-T

http://identifiers.org/hco/6/GRCh38#110299262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40622196-C-A

110299270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622188-A-G

110299284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40622176-T-C

110306678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40621382-T-C

110306740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40621317-C-T

110306889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40621179-A-G

110307140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40620973-T-C

http://identifiers.org/hco/6/GRCh38#110307345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40620783-A-C

110307422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40620712-T-C

110307910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619951-T-C

110307913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619948-T-A

110308113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619745-C-G

110308118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619740-C-T

110308258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619536-A-T

http://identifiers.org/hco/6/GRCh38#110308339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40619460-A-C

110308339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619460-A-G

http://identifiers.org/hco/6/GRCh38#110308430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40619359-C-A

110308725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619079-T-C

110308749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40619067-A-G

110308868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40618974-C-G

110308898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40618944-T-A

110309005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40618825-G-A

http://identifiers.org/hco/6/GRCh38#110309890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40617936-A-C

110310465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40617353-T-C

110310553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40617246-T-C

110310565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40617224-T-G

110311025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40616824-C-T

http://identifiers.org/hco/6/GRCh38#110311260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40616636-C-A

110311359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40616318-T-C

110311402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40616275-C-T

110313541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40616066-A-G

110313918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40615714-T-C

110314767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40614450-A-G

110314778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40614439-A-G

110315144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40614003-G-T

110315190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40613951-C-T

http://identifiers.org/hco/6/GRCh38#110315240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40613906-C-A

110315269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40613883-T-C

110315269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40613883-T-G

110316178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40613038-G-A

110316333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40612892-T-C

http://identifiers.org/hco/6/GRCh38#110316352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40612875-C-A

110316543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40612710-T-A

110316548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40612705-T-G

110317487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40611441-C-G

110317522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40611406-A-G

110317617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40611332-A-G

110317782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40611204-C-T

110317973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610973-G-C

110317980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610966-G-C

110318092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610855-T-C

110318148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610804-C-G

110318184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610765-C-T

110318943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610160-T-C

110319009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40610078-A-T

110319622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40609458-G-C

110319665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40609416-C-T

110319680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40609404-T-C

http://identifiers.org/hco/6/GRCh38#110319823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40609156-C-A

110319998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40609057-C-G

110321661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40607248-C-T

110321854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606965-C-T

110321878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606941-G-A

110322199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606627-G-A

http://identifiers.org/hco/6/GRCh38#110322208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40606618-C-A

110322344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606483-T-C

110322605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606247-T-C

110322688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606174-G-A

110322688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron variant
orthologous variants: 40606174-G-T

110322953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605916-G-A

110322953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605916-G-T

110322991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605888-G-A

110322991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605888-G-T

110323549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605394-A-G

110323616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605327-A-G

110323741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605202-G-A

110323922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40605041-A-T

110324023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40604937-G-A

110324055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40604908-T-C

110324070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40604893-G-A

110324627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40604592-C-G

110324807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40604447-C-T

110327090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40603576-T-C

110327105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40603561-T-C

110327474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40603232-T-C

110327646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40603055-C-T

110327979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602739-C-T

110328050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602674-T-C

110328056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602668-G-A

110328100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602624-T-G

110328475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602266-G-A

http://identifiers.org/hco/6/GRCh38#110328660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40601987-C-A

110328660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601987-C-T

110328680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601967-A-T

110328681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601966-A-G

110328853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601804-T-C

110329156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601375-A-G

110329161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601370-C-T

110329402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601148-T-C

110329485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601080-T-C

110329994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40600638-A-G

110330049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40600589-G-A

110330110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600551-A-G

110330429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600263-T-C

110330443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600249-G-A

110330742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600021-C-G

110330742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600021-C-T

110330932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40598168-T-C

110331035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40598083-G-A

110331393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40597816-A-T

110331655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40597583-G-A

110331655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40597583-G-C

http://identifiers.org/hco/6/GRCh38#110331657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40597581-C-A

110331657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40597581-C-T

http://identifiers.org/hco/6/GRCh38#110332074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40597040-A-C

110332440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596709-C-T

110332536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596612-T-G

110332581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596564-G-A

110332581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596564-G-T

http://identifiers.org/hco/6/GRCh38#110332961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40596493-A-C

110333071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596383-G-A

110333079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596375-A-G

110333145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596327-T-C

110333204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596267-G-A

110333204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596267-G-T

110334059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596176-G-T

http://identifiers.org/hco/6/GRCh38#110334195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40596060-C-A

110334195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596060-C-T

110334252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40596002-A-G

110334349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595939-C-T

110334386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595905-G-A

110334386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595905-G-C

110334544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595735-G-A

110334583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595705-A-G

110334584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595704-G-A

110335054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595256-C-T

110335071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40595239-C-T

110335399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40594927-A-G

110339931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589874-C-T

110340183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589603-T-G

110340222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589555-T-G

110340237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589540-T-C

110340237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589540-T-G

110340242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589522-G-A

110340245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589519-G-T

110340346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589407-G-A

110340518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40589278-G-C

110341153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40587490-T-C

110341161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40587482-G-A

110341488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40587155-C-T

110341507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40587136-C-T

110341590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40587052-T-C

110341959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40586652-G-A

110342049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40586484-G-A

110342088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40586433-C-T

110342126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40586322-T-A

110342383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40586098-T-C

110342388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40586093-T-C

110342388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40586093-T-G

http://identifiers.org/hco/6/GRCh38#110342445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40586019-C-A

http://identifiers.org/hco/6/GRCh38#110342490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40585974-A-C

110342600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40585883-C-G

110342827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40585696-C-T

110342839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40585684-A-G

110342899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40585624-T-C

110343014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40585513-T-A

110348311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40579288-A-G

110348470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40579072-A-G

110348731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40578811-T-A

110349012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40577992-C-T

110349138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40575774-A-G

http://identifiers.org/hco/6/GRCh38#110349768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40574988-C-A

110350053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40574717-A-G

110350390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40574392-A-T

110350452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40574334-T-G

110350619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40567995-C-T

http://identifiers.org/hco/6/GRCh38#110351511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40566874-C-A

110351511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40566874-C-G

110351545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40566823-G-A

110351825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40566546-G-A

110351978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40566434-G-A

110351978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40566434-G-C

110353481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40564170-T-C

110353581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563707-T-A

110353644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563641-G-A

110353728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563564-T-A

http://identifiers.org/hco/6/GRCh38#110353734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40563558-A-C

110353818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563471-A-G

110353915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563370-T-C

110354014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563281-G-T

110354243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40563062-G-A

110354529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40562606-T-A

110354691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562448-T-G

110355109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561904-A-T

110355172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561834-T-C

110355172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561834-T-G

110355186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561820-A-G

110355497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561536-A-G

110355876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561160-C-G

110355903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561140-C-T

110356656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560774-T-C

110356656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560774-T-G

110356913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560530-C-T

110356990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560488-A-T

110357035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560456-G-T

http://identifiers.org/hco/6/GRCh38#110357225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40560260-C-A

110357250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560235-A-T

110357277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560213-G-T

110357281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560209-A-G

110357284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560206-A-G

110357284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560206-A-T

110357446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40560101-G-A

110357446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40560101-G-T

110357459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40560094-G-A

110357459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40560094-G-T

http://identifiers.org/hco/6/GRCh38#110357507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40560025-C-A

110357507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40560025-C-T

http://identifiers.org/hco/6/GRCh38#110357551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559989-C-A

110357551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559989-C-T

110357554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559986-G-A

110357554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559986-G-T

110357718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559873-G-A

110357718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559873-G-T

http://identifiers.org/hco/6/GRCh38#110357730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559861-C-A

110357730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559861-C-T

110357779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559813-G-A

110357779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559813-G-T

110357815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559780-G-A

110357815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559780-G-C

110357815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559780-G-T

110357907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559706-G-A

110357907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559706-G-T

110357913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559700-G-A

110357913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40559700-G-T

http://identifiers.org/hco/6/GRCh38#110357997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559616-C-A

110357997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 40559616-C-G

110357997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 40559616-C-T

110357998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559615-G-A

110357998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559615-G-C

110357998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559615-G-T

http://identifiers.org/hco/6/GRCh38#110358036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559574-A-C

110358036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 40559574-A-G

http://identifiers.org/hco/6/GRCh38#110358076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559534-C-A

110358076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559534-C-T

http://identifiers.org/hco/6/GRCh38#110358081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559529-C-A

110358081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559529-C-G

110358081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 40559529-C-T

http://identifiers.org/hco/6/GRCh38#110358110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559500-C-A

110358110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559500-C-T

110358208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559414-A-G

http://identifiers.org/hco/6/GRCh38#110358232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559390-A-C

110358232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559390-A-G

110358232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559390-A-T

110358256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559366-G-A

110358256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 40559366-G-T

110358278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5 prime UTR variant
orthologous variants: 40559327-T-C

110358322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5 prime UTR variant
orthologous variants: 40559283-G-A

110358322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5 prime UTR variant
orthologous variants: 40559283-G-T

http://identifiers.org/hco/6/GRCh38#110358331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#40559274-C-A

110358331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5 prime UTR variant
orthologous variants: 40559274-C-G

110358331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21566
most severe consequence: 5 prime UTR variant
orthologous variants: 40559274-C-T