http://identifiers.org/hco/9/GRCh38#111360735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58798951-A-C

111360736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58798952-A-T

111360786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58798997-G-A

http://identifiers.org/hco/9/GRCh38#111360846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58799058-C-A

111360846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799058-C-G

111361346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799552-T-C

111361374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799580-G-A

111361399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799601-T-C

111361588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799787-A-G

111361654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799831-T-G

111361803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799954-T-A

111361803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799954-T-C

http://identifiers.org/hco/9/GRCh38#111361827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58799975-C-A

111361827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3 prime UTR variant
orthologous variants: 58799975-C-G

111362245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800350-T-A

111362245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800350-T-C

111362264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800370-A-T

111362265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800371-T-A

111362331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800437-A-G

111362348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800447-A-G

111362578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800657-G-A

111362706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800779-G-C

111362760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800943-C-G

111362760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58800943-C-T

111363099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58801240-C-T

111363129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58801270-T-A

111363129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58801270-T-C

111363129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58801270-T-G

111363310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801469-C-T

111363322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801481-A-G

111363532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801677-T-A

111363667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58801812-G-A

111363667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58801812-G-T

http://identifiers.org/hco/9/GRCh38#111363705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58801848-C-A

111363705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801848-C-T

111363739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801878-A-G

http://identifiers.org/hco/9/GRCh38#111363761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58801893-C-A

111363761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801893-C-G

111363833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58801896-G-A

http://identifiers.org/hco/9/GRCh38#111364009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58801974-C-A

111364193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58802139-G-C

111364381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58802279-T-A

111364381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58802279-T-C

http://identifiers.org/hco/9/GRCh38#111364389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58802287-C-A

111364389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58802287-C-T

111364538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58802612-A-T

111366261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58803692-A-G

111366261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 58803692-A-T

111366270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58803701-A-G

111366303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58803734-A-T

111366305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58803736-G-A

111366305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58803736-G-C

111366305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58803736-G-T

111366340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803769-G-A

111366378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803788-T-A

111366405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803815-T-C

111366458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803858-T-A

111366458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58803858-T-C

111366632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58805649-G-A

111366775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805752-G-A

111367012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805957-G-A

111367012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58805957-G-T

111367081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58806010-T-C

111367226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58806255-G-A

111367364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58806391-C-T

http://identifiers.org/hco/9/GRCh38#111367398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58806424-C-A

111367398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58806424-C-T

111367489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58806495-A-G

111368745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58807228-C-T

111368746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58807229-G-A

111368942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58807657-A-G

111369184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58807900-T-C

111369246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808020-A-G

http://identifiers.org/hco/9/GRCh38#111369253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58808027-C-A

111369259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808028-A-G

111369259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808028-A-T

111369260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808029-G-A

111369260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808029-G-T

111369271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808040-T-A

111369271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58808040-T-C

111370023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809055-T-C

111370037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809069-G-A

111370105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809128-T-C

111370139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809156-T-C

111370316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809301-G-T

111370317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809302-G-C

111370317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809302-G-T

111370327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809312-G-T

http://identifiers.org/hco/9/GRCh38#111370348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58809334-C-A

111370348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58809334-C-T

111370453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58809414-G-C

111370453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58809414-G-T

111370591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58809552-G-A

111370672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58809635-G-A

111370691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58809651-G-A

111370691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58809651-G-T

111370976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58809870-C-T

http://identifiers.org/hco/9/GRCh38#111371738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58810733-C-A

111371994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58810988-A-T

111372357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58811297-A-G

111372655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58811593-A-T

111373171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 58811710-T-C

http://identifiers.org/hco/9/GRCh38#111373257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58811796-A-C

111373431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58811965-T-A

111373443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58811977-T-C

111374071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58812743-G-A

111374071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58812743-G-T

111374188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58812854-T-A

111374350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813014-A-G

111374562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813250-C-T

111374988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813822-T-C

111375012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813851-G-T

111375083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813923-C-G

111375083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813923-C-T

111375084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58813924-A-G

http://identifiers.org/hco/9/GRCh38#111375085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#58813925-C-A

111375094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, undefined
orthologous variants: 58813934-T-C

111375098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, undefined
orthologous variants: 58813938-G-T

111375210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58814089-A-G

111375250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814129-G-A

111375250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814129-G-C

111375250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814129-G-T

http://identifiers.org/hco/9/GRCh38#111375252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58814131-A-C

http://identifiers.org/hco/9/GRCh38#111375270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58814149-A-C

111375290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814170-T-A

111375290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814170-T-C

111375446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814324-A-T

111375534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814394-T-C

111376074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, undefined
orthologous variants: 58814792-A-G

111376093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58814813-T-C

http://identifiers.org/hco/9/GRCh38#111376371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58815153-C-A

111376371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815153-C-G

http://identifiers.org/hco/9/GRCh38#111376373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58815155-C-A

111376375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815157-T-C

http://identifiers.org/hco/9/GRCh38#111376376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58815158-C-A

111376380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815162-T-C

111376425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815207-A-G

111376425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815207-A-T

http://identifiers.org/hco/9/GRCh38#111376452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58815234-C-A

111376452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815234-C-G

111376453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815235-T-C

111376650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815431-A-G

http://identifiers.org/hco/9/GRCh38#111376652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58815433-A-C

http://identifiers.org/hco/9/GRCh38#111376656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58815437-C-A

111376656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815437-C-T

111376740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815513-A-T

111376803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815685-C-T

111376846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815728-A-G

111376998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58815899-C-G

111377676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58817172-T-C

111378799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58817616-T-C

111378802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58817619-G-A

111378802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58817619-G-T

111382988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58818910-G-A

111383006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58818928-C-G

111383006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58818928-C-T

111383007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58818929-G-A

111383076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58818994-A-G

http://identifiers.org/hco/9/GRCh38#111383114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58819039-C-A

111383124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58819048-A-G

111383229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58819161-G-A

111384041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58819644-G-A

111384157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58819752-G-A

111384380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58819981-T-C

111384444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820040-A-G

http://identifiers.org/hco/9/GRCh38#111384490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58820096-A-C

111384490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820096-A-G

111384494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820100-C-G

111384508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820113-G-A

111384514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58820120-G-A

111384514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58820120-G-C

111384542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58820148-C-T

111384575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58820182-A-G

111384579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820186-A-G

111384589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820196-G-A

111384589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820196-G-C

111384654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820245-G-A

111384654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820245-G-T

111384664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820252-G-A

111384664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820252-G-T

111384684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820272-A-G

http://identifiers.org/hco/9/GRCh38#111384689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58820278-A-C

111384689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58820278-A-G

111385090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821043-T-C

111385124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821079-C-G

111385190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821142-C-T

111385205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821163-T-C

http://identifiers.org/hco/9/GRCh38#111385289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58821257-C-A

111385289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821257-C-G

111385307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821295-T-C

111385319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821345-G-A

111385319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821345-G-C

111385319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821345-G-T

http://identifiers.org/hco/9/GRCh38#111385320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58821346-A-C

111385482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821510-G-T

111385497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821525-T-C

http://identifiers.org/hco/9/GRCh38#111385513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58821541-A-C

http://identifiers.org/hco/9/GRCh38#111385533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58821560-C-A

111385533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58821560-C-T

111386342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822006-T-C

111386488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822147-G-A

111386488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822147-G-T

111386594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822214-G-C

111386594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822214-G-T

http://identifiers.org/hco/9/GRCh38#111386596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58822216-C-A

111386627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822249-G-C

111386859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58822417-C-T

http://identifiers.org/hco/9/GRCh38#111389325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58823973-C-A

111389476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824086-T-C

111389537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824147-G-A

111389537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824147-G-C

111389537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824147-G-T

111389829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824452-T-C

http://identifiers.org/hco/9/GRCh38#111389912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58824534-C-A

111389912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824534-C-T

http://identifiers.org/hco/9/GRCh38#111390047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58824761-C-A

111390047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58824761-C-T

111390148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824862-T-A

111390148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824862-T-G

http://identifiers.org/hco/9/GRCh38#111390216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58824930-A-C

111390216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824930-A-G

111390271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58824987-C-T

http://identifiers.org/hco/9/GRCh38#111390750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58825762-C-A

http://identifiers.org/hco/9/GRCh38#111390770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58825779-A-C

111390985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826016-A-G

111391272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826287-G-C

111391272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826287-G-T

http://identifiers.org/hco/9/GRCh38#111391606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58826311-C-A

111391606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826311-C-G

111391606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826311-C-T

http://identifiers.org/hco/9/GRCh38#111391651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58826355-C-A

111391651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826355-C-T

111391742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826388-T-C

http://identifiers.org/hco/9/GRCh38#111391845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58826494-C-A

http://identifiers.org/hco/9/GRCh38#111391886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58826535-A-C

111391941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826574-G-T

111392287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826627-T-C

111392429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826749-C-T

111392593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826898-A-G

111392615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826920-C-T

111392662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826951-A-G

http://identifiers.org/hco/9/GRCh38#111392682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58826963-C-A

111392682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58826963-C-T

http://identifiers.org/hco/9/GRCh38#111392701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58826982-C-A

111392824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58827093-T-C

111392863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58827132-T-C

111392890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58827159-A-G

111393537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58827753-T-C

http://identifiers.org/hco/9/GRCh38#111393581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58827906-C-A

111393581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58827906-C-T

111393610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58827935-T-A

111393619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58827944-G-A

111393619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58827944-G-T

111393730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58828058-T-G

111393807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828138-G-A

111393807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828138-G-T

http://identifiers.org/hco/9/GRCh38#111393812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58828143-C-A

111393844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828176-A-T

111393860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828191-T-G

111393877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828207-G-A

111393877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828207-G-T

http://identifiers.org/hco/9/GRCh38#111393928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58828257-C-A

111393928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828257-C-G

111393943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828273-A-G

111393943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828273-A-T

http://identifiers.org/hco/9/GRCh38#111394015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58828344-A-C

111394015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828344-A-G

111394038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828367-T-G

http://identifiers.org/hco/9/GRCh38#111394089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58828418-C-A

111394089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828418-C-T

http://identifiers.org/hco/9/GRCh38#111394108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58828436-A-C

111394108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58828436-A-G

http://identifiers.org/hco/9/GRCh38#111394271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58828618-C-A

111394271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58828618-C-G

111394271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58828618-C-T

111394274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58828621-C-T

111394310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58828657-G-A

111394310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58828657-G-C

111394310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58828657-G-T

111396228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58829370-T-C

111396627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58829766-T-C

111396995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58830299-G-A

111396995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58830299-G-T

111397403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58830679-C-G

111397446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58830721-G-A

111397529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58830796-T-C

111397569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58830820-G-A

111397917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831114-T-C

111397973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831171-G-A

111397973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831171-G-C

111398200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831387-G-A

111398332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831522-C-T

111398503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831693-G-A

111398503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58831693-G-C

http://identifiers.org/hco/9/GRCh38#111408504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58832663-C-A

111408504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58832663-C-T

http://identifiers.org/hco/9/GRCh38#111408778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58832904-C-A

111408778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58832904-C-T

http://identifiers.org/hco/9/GRCh38#111408781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58832907-C-A

111408781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58832907-C-T

111409052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58833153-G-C

111409912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58833772-A-G

http://identifiers.org/hco/9/GRCh38#111409964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58833846-C-A

111409964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58833846-C-T

111409994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58833881-T-A

111409994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58833881-T-C

111410229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834114-G-T

111410420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834295-T-C

111410893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834410-G-A

111410893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834410-G-C

111410893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834410-G-T

111411059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58834576-T-A

111411285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834788-G-C

111411285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58834788-G-T

http://identifiers.org/hco/9/GRCh38#111411499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58835286-A-C

111411591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835372-G-C

111411591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835372-G-T

http://identifiers.org/hco/9/GRCh38#111411796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58835499-C-A

111411796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835499-C-T

http://identifiers.org/hco/9/GRCh38#111411829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58835533-C-A

111411829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835533-C-T

http://identifiers.org/hco/9/GRCh38#111411860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58835564-C-A

111411860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835564-C-G

111411930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835625-T-A

111411930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58835625-T-C

111412066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58836174-T-C

111412186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58836290-A-G

111412206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58836310-A-T

111412267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58836385-G-A

111412267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58836385-G-T

111412326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58837669-T-C

111412443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58837757-G-A

111412555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58837847-G-T

http://identifiers.org/hco/9/GRCh38#111413120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58838513-C-A

111413163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58838534-C-T

111413428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58840297-A-G

http://identifiers.org/hco/9/GRCh38#111413788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58840565-C-A

111413788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58840565-C-T

111413868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58840640-T-C

111413949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58840729-T-C

111413949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58840729-T-G

111414005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58840785-T-C

111414279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58840986-G-A

111414279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58840986-G-T

111414411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58841364-C-T

111414423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58841377-T-A

111414451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58841405-C-T

111414655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58841609-C-T

111414665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58841619-G-A

111414665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58841619-G-T

111414681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58841709-T-C

111414783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58841869-A-G

111415912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842137-G-A

111415958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842204-C-T

111415961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842207-C-T

111415986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842232-C-T

111416167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842514-A-G

111416167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842514-A-T

111416197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842542-A-G

111416262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58842558-A-G

111417273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58843800-T-C

111417819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844009-A-G

111418053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844249-G-A

111418053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844249-G-C

111418053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844249-G-T

111418549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844688-T-G

111418670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844815-G-A

111418679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58844824-T-C

111418925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58845070-T-C

111419375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58846293-T-G

111419569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58846516-T-A

111420008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58846990-G-C

111420008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58846990-G-T

111420076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58847058-C-G

111420076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58847058-C-T

http://identifiers.org/hco/9/GRCh38#111420282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58847248-C-A

111420479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58847528-G-A

111420636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58847681-T-C

111420751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58847777-T-C

111420974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58847992-T-C

111421281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58848295-T-A

111421458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58848560-G-A

111421558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58848667-A-G

111421800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58848864-T-A

111421800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58848864-T-C

111422239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58849988-T-G

111422417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58850186-T-G

111422827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58850549-T-C

111423171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58850857-A-G

111423171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58850857-A-T

http://identifiers.org/hco/9/GRCh38#111423173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58850859-C-A

111423173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58850859-C-T

111423311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58850998-C-T

111423423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58851090-A-G

111423473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58851125-A-T

111423938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58851559-T-C

111424146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58852282-T-C

111424443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58852541-C-T

http://identifiers.org/hco/9/GRCh38#111424484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58852579-A-C

111424541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58852632-T-C

111425250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58852967-A-G

111425321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58853035-A-G

111425360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58853072-T-C

111425663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58853572-A-T

111425728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58853641-T-C

http://identifiers.org/hco/9/GRCh38#111427943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58861427-C-A

111427943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58861427-C-T

http://identifiers.org/hco/9/GRCh38#111428014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58861493-C-A

111428014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58861493-C-T

111428108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58861591-C-T

111428144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58861627-T-C

111428175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58861658-G-A

111428203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58861684-T-A

111429081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58863036-T-C

111429220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, undefined
orthologous variants: 58863180-C-T

111429508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58863504-T-C

111429598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58863595-C-T

111430063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58863861-A-G

111430194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864004-C-T

111430195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864005-C-T

111430201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864011-C-T

111430245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864055-T-C

111430276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864086-C-T

111430328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864136-C-G

http://identifiers.org/hco/9/GRCh38#111430402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58864211-C-A

111430429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864238-G-A

111430429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864238-G-C

111430429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864238-G-T

111430458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864266-A-T

111430490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864290-G-T

http://identifiers.org/hco/9/GRCh38#111430498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58864298-C-A

111430501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864301-C-T

111430568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58864368-A-G

111430645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864445-C-T

111430684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864484-T-C

111430735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864529-A-T

111430846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864810-C-G

111430924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58864898-G-C

111431108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58865070-C-T

111431201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58865160-T-C

111431260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58865222-T-A

111431260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58865222-T-C

111432655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58868880-A-G

111432662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58868887-C-T

111432735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58868951-A-G

111432745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58868962-T-C

111432783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58868989-T-C

111432825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58869033-C-T

111432854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58869061-A-T

111432945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58869152-T-G

111433158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58869359-A-T

111433181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58869364-T-C

111433212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58869393-A-G

http://identifiers.org/hco/9/GRCh38#111433766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58869931-C-A

111434000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870158-T-C

111434112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870264-T-C

111434139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870295-C-T

111434161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870323-T-C

111434162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870324-G-C

111434393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870555-T-C

111434498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870636-T-C

111434529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870665-T-G

111434687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870777-T-C

http://identifiers.org/hco/9/GRCh38#111434752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58870824-C-A

111434752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870824-C-T

111434862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58870929-T-G

111435299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58871307-A-G

111435390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58871422-T-A

111436547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872241-T-C

111436741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872400-C-T

111436849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872497-T-C

111436850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872498-A-T

111436864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872512-T-G

111436887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872536-T-C

111436897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872546-T-C

111436897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872546-T-G

http://identifiers.org/hco/9/GRCh38#111436928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58872576-C-A

111436928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872576-C-T

111436932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58872580-T-A

111436932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58872580-T-G

111437197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872849-C-G

111437197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58872849-C-T

http://identifiers.org/hco/9/GRCh38#111437200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58872852-C-A

111437515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58873570-A-T

111437870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58874035-T-A

111437870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58874035-T-C

111438940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58874469-A-G

111438953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58874482-G-A

http://identifiers.org/hco/9/GRCh38#111439040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58874562-C-A

111439244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58874757-C-T

http://identifiers.org/hco/9/GRCh38#111440314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58875360-C-A

111440476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58875528-A-G

111440543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875595-T-C

111440553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875605-T-C

111440553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875605-T-G

111440564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875615-G-T

http://identifiers.org/hco/9/GRCh38#111440574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58875625-C-A

111440574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875625-C-T

111440577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875628-G-A

111440577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875628-G-C

111440577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875628-G-T

http://identifiers.org/hco/9/GRCh38#111440603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58875644-C-A

111440603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875644-C-G

111440603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875644-C-T

111440657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875697-T-C

111440683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875723-G-T

111440716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875746-A-G

111440716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58875746-A-T

111441988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58876492-T-A

111441988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58876492-T-C

111442119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58876864-C-G

111442158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58876900-G-T

111442293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877032-G-A

111442293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877032-G-T

111442525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877236-G-C

111442525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877236-G-T

111442798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877470-A-G

111442852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877521-A-G

111443154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877618-T-A

111443567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58877724-A-G

111444344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58878973-T-C

111444369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58879009-A-G

111444582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58879206-G-C

111444582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58879206-G-T

111448557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881242-T-C

111448558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881243-A-T

111448598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881282-G-A

111448610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881294-C-T

111448709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881392-A-G

111448854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881627-C-T

111448861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881633-A-G

111448872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881644-A-G

111448928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58881697-T-C

111449076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58882132-A-G

111449160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58882222-C-T

111449826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58884039-T-A

111450267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58884608-G-T

111451296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885233-C-T

111451302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885239-A-G

111451348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885284-G-T

111451385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885327-A-T

111451461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 58885404-G-A

111451461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 58885404-G-C

111451461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 58885404-G-T

111451704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885644-G-A

111451704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885644-G-T

111451729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885675-A-T

111451738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885687-C-T

111451758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885717-T-C

111451805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885741-G-A

111451805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885741-G-C

http://identifiers.org/hco/9/GRCh38#111451838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58885783-A-C

111452020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58885937-T-C

111452951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58887164-A-G

111452952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58887165-T-C

111453443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58887484-G-A

111453458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58887498-A-G

111453459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58887499-G-A

111454179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58888391-T-C

111454283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58888461-A-G

111459565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58893890-C-T

111460332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58894450-T-C

111467594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58899664-T-C

111467617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58899687-G-A

111467815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58899876-T-G

111468580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902053-A-G

111468624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902108-T-A

111468651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902135-G-A

111468662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902146-T-C

111468676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902155-G-A

111468739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902200-G-A

111468759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902220-G-A

111468771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902228-A-G

111469945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902614-T-C

111470049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902723-C-T

111470088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902744-G-T

111470093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58902749-A-G

111470398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58903156-C-T

111470810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58903530-G-A

111470919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58903679-A-G

111471058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58903802-C-T

111471059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58903803-G-A

111471059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58903803-G-T

http://identifiers.org/hco/9/GRCh38#111471105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58903841-C-A

111471341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58904218-T-C

111471433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58904307-A-G

111471786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58904609-C-T

111472698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58904798-T-C

111473375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58905474-G-A

111473420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58905587-C-T

111474360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58906209-T-G

111474492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58906340-A-G

111474568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58906416-A-G

111474869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58906740-A-T

111474910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58906781-T-C

111474961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58906838-T-C

111475959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907498-T-G

111475961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907500-G-A

111476050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907590-G-A

111476051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907591-A-G

111476148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907679-T-A

111476148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907679-T-C

111476225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907752-C-G

111476266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58907793-T-C

http://identifiers.org/hco/9/GRCh38#111477631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58908202-A-C

111477765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58908326-G-A

111480772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909369-C-T

111481054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909645-G-A

111481054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909645-G-T

111481057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909648-T-C

111481165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909781-T-C

111481165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909781-T-G

111481171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909787-G-T

111481260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58909831-G-T

111481934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58910264-G-A

111482110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58910436-G-A

111482161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58910499-G-A

111482201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58910543-G-A

111482242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58910594-T-A

http://identifiers.org/hco/9/GRCh38#111482533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58910879-A-C

111482554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58910905-G-C

111482833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911165-G-C

111482976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911322-C-T

111483147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911499-C-T

http://identifiers.org/hco/9/GRCh38#111483222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58911571-C-A

111483377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58911733-T-C

http://identifiers.org/hco/9/GRCh38#111483420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58911781-C-A

111483420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911781-C-T

111483441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911807-G-A

111483441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911807-G-T

111483442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911808-G-A

111483442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911808-G-C

111483442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911808-G-T

111483471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911837-G-A

111483471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911837-G-C

111483471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911837-G-T

111483477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911843-G-A

111483477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58911843-G-T

http://identifiers.org/hco/9/GRCh38#111483633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58912032-C-A

111483633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58912032-C-G

111483633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58912032-C-T

111483660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58912058-G-T

111483774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912169-G-C

111483774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912169-G-T

111483806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912186-T-C

111483811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912191-G-A

111483811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912191-G-C

111483811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912191-G-T

http://identifiers.org/hco/9/GRCh38#111483915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58912283-C-A

111483915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912283-C-T

111483933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912306-G-A

111483933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912306-G-T

http://identifiers.org/hco/9/GRCh38#111483947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58912324-C-A

111483947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912324-C-G

111483947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912324-C-T

111483967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912348-G-A

111483967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron variant
orthologous variants: 58912348-G-T

111484200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 58912541-G-A

111484200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 58912541-G-C

111484200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 58912541-G-T

111484255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 58912599-G-A

111484255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 58912599-G-T

http://identifiers.org/hco/9/GRCh38#111484260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58912604-C-A

111484260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 58912604-C-T

111484261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 58912605-C-T

111484267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 58912611-G-T

111484335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58912674-G-A

111484382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 58912723-T-C

111484452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: stop gained
orthologous variants: 58912809-G-A

111484452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58912809-G-C

111484452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58912809-G-T

111484458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58912815-G-A

111484497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58912843-G-T

111484533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58912894-G-C

111484534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: synonymous variant
orthologous variants: 58912895-G-A

111484534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58912895-G-C

http://identifiers.org/hco/9/GRCh38#111484553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#58912920-C-A

111484723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29020
most severe consequence: missense variant
orthologous variants: 58913037-C-T