94567429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94426518-T-G

94567460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94426487-A-T

94567623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94426300-A-G

94567675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94426254-C-T

http://identifiers.org/hco/12/GRCh38#94567678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94426251-C-A

http://identifiers.org/hco/12/GRCh38#94567706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94426233-C-A

94567749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94426202-A-G

94567782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94426169-T-C

94567935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425967-A-G

94567943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425959-G-A

94567993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425906-G-A

94568134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425829-T-C

94568173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425808-C-T

94568252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425720-A-G

94568252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425720-A-T

94568429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425571-G-T

94568577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94425427-A-G

http://identifiers.org/hco/12/GRCh38#94568857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94425150-C-A

http://identifiers.org/hco/12/GRCh38#94568922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94425084-C-A

http://identifiers.org/hco/12/GRCh38#94569003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94425017-C-A

94569161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424856-G-A

94569161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424856-G-T

94569180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424826-G-A

http://identifiers.org/hco/12/GRCh38#94569209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94424797-C-A

94569209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424797-C-T

http://identifiers.org/hco/12/GRCh38#94569362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94424670-C-A

http://identifiers.org/hco/12/GRCh38#94569469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94424613-C-A

94569546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424546-A-G

http://identifiers.org/hco/12/GRCh38#94569855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94424235-C-A

94569891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424195-G-T

94569967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94424111-G-T

http://identifiers.org/hco/12/GRCh38#94570051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94424051-C-A

http://identifiers.org/hco/12/GRCh38#94570132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423972-C-A

94570167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423941-T-C

http://identifiers.org/hco/12/GRCh38#94570293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423811-C-A

94570293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423811-C-T

94570353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423750-C-T

http://identifiers.org/hco/12/GRCh38#94570398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423701-C-A

94570466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423633-C-T

http://identifiers.org/hco/12/GRCh38#94570779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423482-C-A

94570779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423482-C-T

94571045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423221-G-A

94571045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423221-G-T

http://identifiers.org/hco/12/GRCh38#94571062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423204-C-A

http://identifiers.org/hco/12/GRCh38#94571168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423161-C-A

http://identifiers.org/hco/12/GRCh38#94571217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423111-A-C

94571230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94423097-C-T

94571261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94423066-G-A

94571261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94423066-G-T

94571270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94423057-G-A

94571270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94423057-G-T

http://identifiers.org/hco/12/GRCh38#94571280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423047-A-C

94571280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94423047-A-G

94571280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94423047-A-T

94571309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94423019-A-G

http://identifiers.org/hco/12/GRCh38#94571310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#94423018-C-A

94571310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94423018-C-T

94571382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94422943-A-G

94571428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94422896-A-G

94571430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 3 prime UTR variant
orthologous variants: 94422894-T-C

94571556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94422769-G-T

94571598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense_variant, undefined
orthologous variants: 94422727-A-G

94572005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94422350-T-C

94572125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94422257-A-G

94572161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94422206-G-C

94572186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94422177-G-C

http://identifiers.org/hco/12/GRCh38#94574406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94421035-A-C

94574406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94421035-A-T

94574513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94420937-G-A

94574879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94420564-C-T

94574888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94420557-C-T

94576221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94419379-G-A

94577036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418874-G-C

94578292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418366-G-T

http://identifiers.org/hco/12/GRCh38#94578294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94418364-C-A

http://identifiers.org/hco/12/GRCh38#94578316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94418347-C-A

94578316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418347-C-T

94578350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418313-C-G

94578350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418313-C-T

94578398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94418265-A-G

94578440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94418223-T-G

94578571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418083-G-A

94578571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94418083-G-T

94578664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417998-G-T

94578768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417894-C-T

94578897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417749-T-C

94578910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417736-T-A

94578943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417704-G-C

94579333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417362-C-T

94579623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417147-C-T

94579783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94417013-C-T

94579931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94416873-C-T

94580176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94416137-A-G

94580385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94415985-T-A

94581805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94415016-T-C

94581820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94415001-T-A

94581820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94415001-T-C

94581835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414986-G-A

94581888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: synonymous variant
orthologous variants: 94414933-A-G

94581889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414932-G-A

94581919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414902-T-C

94582186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414635-T-C

94582261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414560-T-C

94582300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414521-T-A

94582300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414521-T-C

94582366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414455-A-G

94582406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: synonymous variant
orthologous variants: 94414415-G-A

94582406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: missense variant
orthologous variants: 94414415-G-C

94582590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94414236-T-A

http://identifiers.org/hco/12/GRCh38#94582609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94414214-C-A

94582609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94414214-C-T

94582645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94414179-G-A

94582645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94414179-G-C

94582645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94414179-G-T

94582656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94414168-G-T

94582918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94413926-G-A

94583580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94413478-G-A

http://identifiers.org/hco/12/GRCh38#94583921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94413131-A-C

94584513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412960-C-T

94584514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412959-T-C

http://identifiers.org/hco/12/GRCh38#94584535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94412939-C-A

94584535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412939-C-T

94584634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412852-G-A

94584756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412721-A-G

http://identifiers.org/hco/12/GRCh38#94584948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94412548-C-A

94584948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412548-C-G

http://identifiers.org/hco/12/GRCh38#94585062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94412430-A-C

94585100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412393-T-G

94585172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412342-T-C

94585358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412208-C-T

94585716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412160-T-C

http://identifiers.org/hco/12/GRCh38#94585752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94412128-C-A

94585772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94412112-C-T

94585911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94411965-T-G

94585986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94411894-C-T

94586493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94411448-A-G

94586533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94411407-G-A

94586931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94410981-G-A

94586931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94410981-G-T

http://identifiers.org/hco/12/GRCh38#94587210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94410733-A-C

94587303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94410634-T-C

94587783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94409161-G-A

94587795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94409149-G-A

94587920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94409008-T-C

94587949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94408974-C-G

94588581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: -T-A

94588581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/12/GRCh38#94589667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94407327-A-C

94589683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94407311-C-T

94589796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94407211-A-G

94589965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94407059-T-C

94591986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94406016-A-G

94592042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405961-A-G

http://identifiers.org/hco/12/GRCh38#94592054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94405953-C-A

94592076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405931-G-A

94592152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405861-T-C

94593756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405432-C-T

94593858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405324-G-A

94593858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405324-G-C

http://identifiers.org/hco/12/GRCh38#94594110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94405102-A-C

94594112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94405100-T-C

94594421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404969-C-T

94594468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404922-G-A

94594636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404804-G-A

94594679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404727-G-A

94594687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404719-T-C

94596499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404130-T-C

94596586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94404071-C-T

94598008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94402216-C-G

94598576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401873-G-T

94598744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401707-G-A

94598744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401707-G-C

94598763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401686-G-A

94598769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401685-C-T

94598809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401650-C-T

94598810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401649-G-A

94598811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401648-A-G

94599003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94401459-C-T

94602271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94399655-G-C

94602454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94399462-C-T

94602572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94399347-G-A

94602910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94398797-C-G

94603083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94398672-A-T

94603401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94398435-G-T

http://identifiers.org/hco/12/GRCh38#94603473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94398373-C-A

http://identifiers.org/hco/12/GRCh38#94603620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94398274-A-C

94604004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94397927-A-G

94604060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94397852-G-A

94604060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94397852-G-T

http://identifiers.org/hco/12/GRCh38#94604308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94397603-C-A

http://identifiers.org/hco/12/GRCh38#94604309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94397602-C-A

http://identifiers.org/hco/12/GRCh38#94604466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94397440-C-A

94604466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94397440-C-T

94605409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94396204-G-A

94605592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94396032-C-T

94605608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94396016-T-C

94605610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94396014-C-T

94606055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94395301-G-A

94607765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394949-A-G

http://identifiers.org/hco/12/GRCh38#94608198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94394501-A-C

94608219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394481-G-A

94608219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394481-G-T

94608266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394432-T-C

94608393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394105-T-G

94608445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394059-C-T

94608453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394045-T-A

94608453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94394045-T-C

94608727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94393775-C-G

94608750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94393747-C-G

94608750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94393747-C-T

94608800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94393706-T-C

94610137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393635-G-A

94610137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393635-G-C

94610263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393511-C-T

http://identifiers.org/hco/12/GRCh38#94611011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94392192-A-C

http://identifiers.org/hco/12/GRCh38#94611407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94391822-C-A

94611478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94391749-T-C

http://identifiers.org/hco/12/GRCh38#94612856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94389765-C-A

94613044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389605-G-C

94613054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389598-T-C

94613201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389458-C-T

http://identifiers.org/hco/12/GRCh38#94613803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94389033-C-A

94614456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94388327-G-A

94614537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94388258-T-A

94614537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94388258-T-C

94614539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94388247-T-C

94614672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94388106-T-G

94614726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94388052-T-C

94615394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387401-A-T

94615414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387381-C-T

94615576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387236-G-A

94615576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387236-G-C

94615666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387145-C-T

94615678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387133-T-A

94615905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386905-A-G

http://identifiers.org/hco/12/GRCh38#94615923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94386886-C-A

94616059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94386754-T-G

94616280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94386540-G-A

94616280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94386540-G-T

94616319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94386494-C-T

http://identifiers.org/hco/12/GRCh38#94616321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94386492-A-C

94616336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, undefined
orthologous variants: 94386478-T-C

94616338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, undefined
orthologous variants: 94386476-G-A

94616338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, undefined
orthologous variants: 94386476-G-C

94616339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, undefined
orthologous variants: 94386475-G-A

94616357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94386457-G-T

94616415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 94386109-A-G

94616706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, undefined
orthologous variants: 94385842-G-C

http://identifiers.org/hco/12/GRCh38#94617287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94385311-C-A

94617287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94385311-C-T

94617750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94384836-T-C

94617777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94384812-G-A

94620710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382787-A-T

94620759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382740-T-A

94620759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382740-T-C

94621083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382383-T-G

94621185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382280-C-T

94621260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382232-G-C

94621260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94382232-G-T

94621500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94381978-C-G

94621931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94381546-A-G

94622574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94380906-T-C

94622780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94380666-T-A

94622782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94380664-T-A

94622782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94380664-T-C

94622790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94380656-G-A

94622945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94380453-C-T

94626602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94376696-C-T

94627153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94376366-G-A

94627493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94376183-T-A

94627605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94376069-G-A

94627605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94376069-G-C

http://identifiers.org/hco/12/GRCh38#94627670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94376019-A-C

http://identifiers.org/hco/12/GRCh38#94627690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94376003-C-A

http://identifiers.org/hco/12/GRCh38#94627890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94375818-C-A

94627907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375806-G-A

94627907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375806-G-C

94627940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375773-G-A

94628083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375624-G-A

94628130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375575-G-A

94628154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375551-G-A

94628154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375551-G-T

94628178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94375539-T-C

94628598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94374214-G-A

94628651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94374153-C-T

94628768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94374039-A-G

94628965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94373842-T-C

94629102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94373714-T-C

94629309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94373499-C-T

94629341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94373467-G-C

94629420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94373388-A-G

94629597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94373237-T-G

http://identifiers.org/hco/12/GRCh38#94631501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94371166-C-A

94631507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94371160-C-T

94631625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94371077-T-C

94631742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94370978-T-C

94631931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94370802-A-G

94632075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94370599-C-T

94632292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94370263-T-C

94632368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94370184-G-C

94632594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94369973-A-G

94633173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94369484-T-C

94633239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94369450-C-T

94633428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94369310-G-C

94633554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94369164-C-T

94633684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94369023-T-C

94633837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94368886-C-T

94633854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94368869-T-C

94633866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94368861-G-A

94634830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94368465-T-C

94634880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94368417-G-A

94635075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94368235-A-G

94635733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94367471-G-A

94635810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94367422-G-A

94635816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94367411-G-A

94636137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94367163-G-A

94636474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94366811-G-C

94636598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94366683-A-G

94636657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94366641-G-T

94636717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94366589-T-C

94637399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94365907-G-C

94637971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94365439-G-A

94638026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94365387-C-T

94638061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94365356-A-G

94638098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94365314-G-A

94638110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94365302-T-C

94638292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94363251-C-G

94638292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94363251-C-T

http://identifiers.org/hco/12/GRCh38#94638384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94363166-A-C

94638665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94362901-C-G

94639124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94362416-C-T

94639227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94362311-C-G

http://identifiers.org/hco/12/GRCh38#94639800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94361626-A-C

94639840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94361593-G-A

94639840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94361593-G-C

94639850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94361582-C-T

94640069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94361412-C-T

94640586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94361208-G-A

94641673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94359929-A-T

94641782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94359811-A-G

94642469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94358140-T-C

94642764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357912-T-G

94642872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357803-T-C

94642872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357803-T-G

94642873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357802-G-T

http://identifiers.org/hco/12/GRCh38#94642878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94357797-C-A

94643418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357591-C-T

94643429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357580-T-C

94643464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94357545-C-T

94644023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356799-A-T

94644343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356451-T-C

94644464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356350-C-T

94644492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356316-T-A

94644492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356316-T-C

http://identifiers.org/hco/12/GRCh38#94644501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94356305-C-A

94644501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356305-C-T

94644552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356239-G-A

94644592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94356171-T-C

94644984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94355825-T-G

94645089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron variant
orthologous variants: 94355723-C-T

http://identifiers.org/hco/12/GRCh38#94647275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94353585-C-A

94647484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94353387-T-C

94647619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94353271-T-A

94647708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94353174-T-A

94648779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94352321-C-T

94648807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94352293-T-C

94648872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94352211-T-C

94649007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94352075-T-C

94649612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351532-C-T

94649788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351381-C-T

http://identifiers.org/hco/12/GRCh38#94649898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94351294-C-A

94649998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351214-C-G

94650197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351091-T-A

94650220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351088-C-G

94650220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351088-C-T

http://identifiers.org/hco/12/GRCh38#94650249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#94351073-C-A

94650249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94351073-C-T

94650259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351063-C-G

94650262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351060-G-C

94650263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351059-G-A

94650263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351059-G-C

94650263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351059-G-T

94650271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351051-G-T

94650274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351048-T-G

http://identifiers.org/hco/12/GRCh38#94650286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94351031-C-A

94650286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351031-C-G

http://identifiers.org/hco/12/GRCh38#94650291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94351026-C-A

http://identifiers.org/hco/12/GRCh38#94650322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94350995-C-A

94650322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350995-C-T

94650327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350990-G-A

94650327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350990-G-C

94650327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350990-G-T

http://identifiers.org/hco/12/GRCh38#94650366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94350951-C-A

94650366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94350951-C-G

94650366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94350951-C-T

http://identifiers.org/hco/12/GRCh38#94650395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#94350922-C-A

94650395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94350922-C-T

94650411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94350906-G-A

94650411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94350906-G-C

94650411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94350906-G-T

94650537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29199
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94350762-G-A