44110506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77053292-T-C

44110893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053184-C-G

44110990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053085-C-T

44111001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053074-T-A

http://identifiers.org/hco/13/GRCh38#44111189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77052900-C-A

44111189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052900-C-T

44111219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052860-C-G

44111475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052587-T-C

http://identifiers.org/hco/13/GRCh38#44111477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77052585-C-A

44111477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052585-C-T

44111565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052493-A-G

44111669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052394-A-G

44111669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052394-A-T

44111686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052376-G-T

44112012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052008-G-A

44112012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052008-G-T

http://identifiers.org/hco/13/GRCh38#44112088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77051931-A-C

44112398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051623-T-A

44112398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051623-T-C

44112573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051468-C-T

44112841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051204-T-C

44112927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051112-G-A

44114998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77050172-T-C

44115244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049939-G-A

44115429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049756-C-T

44115706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049461-T-C

44115801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049321-T-C

44116043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049063-T-G

44116080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049024-G-C

44116095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049009-C-G

44116181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048901-G-T

44116194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048888-A-G

44116568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048367-A-G

44116644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048290-G-A

44116681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048249-G-A

44116710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048164-G-A

44116712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048162-G-C

http://identifiers.org/hco/13/GRCh38#44116749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77048125-A-C

44116895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77047998-T-C

http://identifiers.org/hco/13/GRCh38#44116929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77047967-C-A

44116929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77047967-C-T

44116987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77047918-T-G

http://identifiers.org/hco/13/GRCh38#44117252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77042390-A-C

44117258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77042384-T-A

http://identifiers.org/hco/13/GRCh38#44117759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77041889-A-C

44117759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041889-A-T

44117762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041886-G-A

44118161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041540-G-C

44118199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041511-G-A

44118256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041454-T-C

44118256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041454-T-G

44118288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041422-C-T

44118372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041358-A-G

44118385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041345-T-C

44118405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041326-C-T

44118559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041172-T-C

44118563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041168-G-C

44118745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041041-G-A

44118985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77040799-G-A

44119036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77038994-G-C

44119106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038931-T-C

44119164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038900-A-T

44119284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038778-G-A

44119349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038714-T-A

44119364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038699-G-C

44119412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038663-G-A

44119508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038537-T-C

44119976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77037733-A-G

44120076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77037635-A-T

44120443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77037279-A-G

44121269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77036483-C-T

http://identifiers.org/hco/13/GRCh38#44121412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77036347-C-A

44121412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77036347-C-G

44121438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77036321-C-T

44124638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77031092-C-T

44124682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77031027-A-G

44124717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030992-G-A

44124717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030992-G-T

44125353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030409-A-T

44125919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030284-C-T

44126100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030129-T-A

44126196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030044-T-C

44126274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029966-C-T

44126296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029941-A-G

44126511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029711-A-G

44126563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029665-C-T

44126733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029523-A-G

http://identifiers.org/hco/13/GRCh38#44127085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77029168-C-A

44127532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029016-C-T

http://identifiers.org/hco/13/GRCh38#44127893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77027816-C-A

44128004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027715-G-A

44128202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027537-T-C

44128392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027365-T-C

http://identifiers.org/hco/13/GRCh38#44128526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77027230-C-A

44128633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027126-C-T

44128874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77026883-G-A

44128983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77026752-C-T

44129426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77026418-G-T

44132790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77025296-C-G

44133066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77025071-G-A

44133130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77025012-A-G

44133694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77024232-G-T

44135105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023314-T-C

44135259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023162-G-T

44135295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023130-A-G

44135351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023084-G-A

44135752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77022756-G-T

44135776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77022732-T-A

44135794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77022715-A-G

44136220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018973-A-G

44136429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018768-T-C

44136460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018737-T-C

44136598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018613-G-A

44136709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018490-G-T

44137035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018186-A-G

44137128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77018107-A-G

44137300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017944-A-G

44137486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017778-G-A

44137689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017583-A-G

44137770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017117-T-C

44137800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017087-C-T

44139152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77016393-C-G

44139553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77016011-G-T

44139656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77015914-G-T

44139844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77015678-T-C

44140801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77014842-C-T

44141018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77014634-G-T

44141202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77014462-A-G

44141430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77014220-C-G

44142738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77013839-T-C

44142778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77013817-G-T

44142800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77013795-A-G

44143192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77013355-G-A

44143520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77013030-T-C

44143742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77012834-G-T

44143949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77012671-G-A

44144014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77012615-A-T

44145730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77011460-A-G

44145760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77011431-A-G

44146967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77011142-G-A

44146967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77011142-G-T

http://identifiers.org/hco/13/GRCh38#44146968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77011141-C-A

http://identifiers.org/hco/13/GRCh38#44146980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77011130-C-A

44146980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77011130-C-T

http://identifiers.org/hco/13/GRCh38#44147000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77011118-A-C

44147170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010960-C-T

44147213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010917-C-T

44147269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010874-A-G

44147293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010850-T-C

44148175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77009989-A-G

44148226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77009951-T-A

44148370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77009844-C-T

http://identifiers.org/hco/13/GRCh38#44148447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77009770-C-A

44148593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77009623-C-T

44149764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77009080-T-A

44149765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77009079-A-T

44149931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77008896-T-G

44150143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77008287-C-T

44150595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77007872-A-T

44150615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77007861-G-A

44150643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77007830-C-T

44150842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77007553-C-G

http://identifiers.org/hco/13/GRCh38#44150984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77007404-C-A

44150984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77007404-C-T

44151349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005919-T-C

44151453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005818-C-T

44151579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005684-T-A

44151579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005684-T-C

44151625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005638-G-A

44151675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005593-A-G

44151699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005568-G-A

44151852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005418-A-G

44151878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005392-G-A

44152075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77005164-T-C

44153219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77004138-A-G

44153342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77004040-G-A

44153346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77004036-G-A

http://identifiers.org/hco/13/GRCh38#44153347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77004035-A-C

44153347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77004035-A-T

44153585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77003773-G-A

44153585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77003773-G-T

44153934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77003469-T-C

44153966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77003439-T-C

44153974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77003431-C-T

44154029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77003355-G-T

44154173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77003202-T-C

44154179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77003196-C-T

44155343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002983-G-A

44155397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002930-T-C

http://identifiers.org/hco/13/GRCh38#44156009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77002292-A-C

44156060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002237-G-A

44156137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77002167-C-T

44157550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001323-T-C

44157618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001271-T-C

44157718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001184-C-T

44157722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001180-G-A

44157857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001068-G-A

44157876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77001047-T-C

44158047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77000940-A-T

44158071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77000916-G-A

44158130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77000858-C-T

44158292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77000658-G-T

44158339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77000617-C-T

44158768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77000290-T-C

44158947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77000117-C-T

44159075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999986-G-T

44159292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999792-G-A

44159612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999482-C-T

44159713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999391-C-T

44159799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999305-G-A

44159855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999249-C-T

44159953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999161-A-G

44159981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999133-T-C

44160210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998917-C-G

44160344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998745-A-G

44160344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998745-A-T

44160462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998645-T-G

44160482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998627-A-T

44160533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998591-T-A

44160533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998591-T-C

44160688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76998443-G-A

44160920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76998203-A-G

http://identifiers.org/hco/13/GRCh38#44161055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76998069-C-A

44161055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998069-C-T

http://identifiers.org/hco/13/GRCh38#44161143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76997995-A-C

44161143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76997995-A-T

http://identifiers.org/hco/13/GRCh38#44161144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76997994-C-A

44161144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76997994-C-G

44161144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76997994-C-T

44161173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76997965-G-A

44161173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76997965-G-T

44161193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76997945-G-A

44161193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76997945-G-T

44161824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76997724-C-G

44162364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76997228-T-A

44162542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76997087-A-G

http://identifiers.org/hco/13/GRCh38#44162611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76997020-A-C

44162611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76997020-A-G

44163433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76996190-C-T

44163534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76996034-G-A

44163534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76996034-G-C

44164498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76995733-C-G

44164607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76995637-T-C

44165980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76993433-G-A

44165980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76993433-G-C

44176054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76992316-T-C

44177255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76990579-A-G

44177292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76990543-T-G

44177381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76990438-C-G

44177819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76990108-G-A

http://identifiers.org/hco/13/GRCh38#44179034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76989292-C-A

44179288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76989050-G-A

44179310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76989031-G-A

http://identifiers.org/hco/13/GRCh38#44179725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76988728-C-A

44179847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988638-A-G

44180090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988395-A-G

44180226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987610-C-T

44180438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987522-C-T

44180562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987392-C-G

44180562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987392-C-T

44180674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987280-G-A

44180824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987119-A-G

44180866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987087-C-T

44180905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987050-G-C

44180921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987034-A-G

44180950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987005-T-C

44181085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986868-G-T

44181126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986828-A-G

44181184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986770-G-T

44181203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986753-A-G

44181285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986676-C-T

44181722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986563-C-T

44181774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986511-C-T

44181955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986360-C-G

44181984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986353-G-T

44182064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986277-T-A

44182121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986229-C-T

http://identifiers.org/hco/13/GRCh38#44182163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76986198-C-A

44182177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986187-A-G

44182277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986078-T-C

44185456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76984664-A-G

44185482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76984649-G-A

44185646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76984502-A-G

44185968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76984150-T-A

44185968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76984150-T-C

44186202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983940-G-T

44186480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983680-C-G

44186480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983680-C-T

http://identifiers.org/hco/13/GRCh38#44186536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76983625-C-A

44186537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983624-A-T

44186608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983531-A-G

44186626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983517-A-G

44186638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983505-A-G

44186654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983131-G-A

44186791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76983003-C-T

44186798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76982996-C-T

44186828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76982967-T-A

44186844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76982951-C-T

44186946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76982854-T-A

44187021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76982738-T-C

44187233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76981672-G-A

44187246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76981659-T-C

44187393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76981518-C-T

44187489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76981421-G-A

44187501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76981409-C-T

44187682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76981248-G-A

44187872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76980481-A-G

44187924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76980418-G-A

http://identifiers.org/hco/13/GRCh38#44188105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76980224-A-C

44188349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76980000-G-C

44188418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76979932-A-G

http://identifiers.org/hco/13/GRCh38#44188704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76979705-C-A

44188778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76979631-A-G

44190751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76978834-A-G

44191094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76978496-A-T

http://identifiers.org/hco/13/GRCh38#44191109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76978481-C-A

44191258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76978325-A-G

44191367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76978255-G-A

44191452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76978124-G-C

44191631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76977941-G-A

44191631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76977941-G-C

44191691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76977907-C-T

44191772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76977829-A-G

44191841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76977757-A-T

44191920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76977674-T-G

44192028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76977566-C-G

44192248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76977416-A-G

http://identifiers.org/hco/13/GRCh38#44192282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76977409-A-C

44192602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76977156-G-A

44192740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76977004-A-G

44192752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976992-A-T

http://identifiers.org/hco/13/GRCh38#44192809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76976939-C-A

44192827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976921-C-G

http://identifiers.org/hco/13/GRCh38#44193064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76976613-A-C

44193178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976486-C-T

44193187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976477-T-C

44193194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976470-C-T

44193198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976466-G-A

44193396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76976293-A-T

44193618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76975909-T-C

http://identifiers.org/hco/13/GRCh38#44193942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76975634-C-A

44193942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76975634-C-T

44194123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76975476-T-C

44195689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76975158-C-T

44195703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76975144-C-G

44195842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76975018-G-A

http://identifiers.org/hco/13/GRCh38#44195863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76974999-C-A

44195863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974999-C-G

44195939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974930-T-C

44195999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974882-G-T

44196021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76974856-G-T

http://identifiers.org/hco/13/GRCh38#44196063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76974814-C-A

44196063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76974814-C-T

44196075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76974802-G-T

44196126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76974768-C-T

http://identifiers.org/hco/13/GRCh38#44196129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76974765-C-A

44196234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76974687-G-A

44196234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76974687-G-T

44196367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974584-G-A

44196367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974584-G-T

44196376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974575-T-C

44196434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76974521-C-T

44196608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76973869-C-G

44196639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76973838-T-C

44196853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76973636-G-T

http://identifiers.org/hco/13/GRCh38#44196885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76973602-C-A

http://identifiers.org/hco/13/GRCh38#44196890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76973597-C-A

44196890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76973597-C-T

http://identifiers.org/hco/13/GRCh38#44196905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76973582-C-A

44196944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76973543-G-A

44196944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76973543-G-T

44197031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76973443-T-C

44197250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76972011-A-G

44197266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76971994-T-C

44197304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971951-T-C

44197307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971950-G-A

44197307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971950-G-T

44197331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971928-A-G

44197391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971861-A-G

44197559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971638-G-A

44197628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971577-C-T

44197684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971537-C-G

44197684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971537-C-T

44197769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971453-T-G

44197778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971444-C-T

44197816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971407-A-G

44198148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76971061-A-G

44198235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76970975-G-T

44198486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76970735-C-T

44198611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76970608-G-A

44198648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76970572-T-C

44199034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76970042-C-G

44199034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76970042-C-T

44199093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969978-T-A

44199114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969957-C-G

44199138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969934-G-A

44199243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969838-C-T

44199292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969799-T-C

http://identifiers.org/hco/13/GRCh38#44199426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76969678-A-C

44199568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969508-G-A

44199661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969409-A-T

44199707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76969367-C-G

44199948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76969121-A-G

44200404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76968375-G-T

44200421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76968364-G-C

44200428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76968357-A-G

http://identifiers.org/hco/13/GRCh38#44200576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76968209-C-A

44200821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76967976-G-A

44200869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76967930-C-T

44201061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76967747-C-G

44201061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76967747-C-T

44201220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76967446-G-A

44201548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76967144-C-G

44208791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76964584-G-T

44209329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76964033-A-G

44209484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963895-T-C

44209551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963816-C-G

44209568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963798-G-T

44209717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963652-C-T

44209767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963602-C-T

44209948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963436-C-T

44209990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963392-C-T

http://identifiers.org/hco/13/GRCh38#44210567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76963019-C-A

http://identifiers.org/hco/13/GRCh38#44211118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76962371-C-A

44211188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76962301-G-C

44211542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961951-G-A

44211563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961930-C-T

44211704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961416-G-A

44211704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961416-G-T

44211712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961408-C-G

44211727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961393-C-T

44211782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961346-C-T

44211844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961281-A-T

44211969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961178-G-A

44211969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961178-G-T

http://identifiers.org/hco/13/GRCh38#44212039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76961111-C-A

44212039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961111-C-T

http://identifiers.org/hco/13/GRCh38#44212382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76960777-C-A

44212382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76960777-C-T

44212805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76960355-C-T

44213426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76959799-G-A

http://identifiers.org/hco/13/GRCh38#44213463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76959762-C-A

44214695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76959361-A-G

44215195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958906-G-T

44215218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958894-G-A

44215365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958798-A-G

http://identifiers.org/hco/13/GRCh38#44215402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76958768-C-A

44215415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958755-T-G

44216702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953750-C-T

44216839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953616-T-C

44216963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953530-T-A

44218367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952899-T-A

44218367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952899-T-C

44218598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952665-G-A

44218655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952609-A-G

http://identifiers.org/hco/13/GRCh38#44218729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76952539-A-C

44218961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952327-T-C

44219013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952275-C-T

44219201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952095-G-A

44219813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76951687-T-G

44219962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76951544-C-T

44220092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76951448-C-T

http://identifiers.org/hco/13/GRCh38#44221059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76950041-A-C

44221059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76950041-A-G

44221063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76950037-C-T

44221127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949974-T-C

44221211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949893-C-T

44221283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949845-C-G

44221319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949809-C-T

44221350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949779-C-T

44221461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949668-G-A

44221541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949579-C-G

44221556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949536-G-A

44221729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949274-G-A

44221729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949274-G-T

44221837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949161-A-G

44221955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949050-C-T

44223836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76947133-G-A

44223902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76947074-C-T

44223991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946943-G-T

44224120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946806-G-A

44224233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946706-T-C

http://identifiers.org/hco/13/GRCh38#44224299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76946580-A-C

44224739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946140-G-A

http://identifiers.org/hco/13/GRCh38#44224880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76945990-A-C

44224906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945965-G-A

44224906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945965-G-C

44225107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945804-T-C

44225174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945744-C-T

44225319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945621-G-A

44225319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945621-G-T

44225658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945280-A-G

44225880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945147-G-A

44226164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76944157-T-C

44226390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943938-A-G

44226490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943855-C-T

44226527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943818-G-A

44226594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943751-T-C

44226860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943494-T-C

44227287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942747-G-A

44227356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942701-T-C

44227368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942689-G-A

44227376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942681-G-T

44227478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76941633-T-G

44227508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76941604-T-C

44227609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76941527-C-T

44227701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76941446-C-T

http://identifiers.org/hco/13/GRCh38#44228099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76941135-C-A

44228255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940978-C-T

44228415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940806-T-C

44228415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940806-T-G

44228534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940688-G-A

44228550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940672-T-C

http://identifiers.org/hco/13/GRCh38#44228657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76940588-C-A

44228747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940503-G-C

44228906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940365-G-A

44228906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940365-G-T

44228975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940329-G-T

44229095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940206-T-C

44229230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940065-C-G

44229267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76940027-C-T

44229304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76939993-G-C

44229676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76939723-T-C

http://identifiers.org/hco/13/GRCh38#44229750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76939686-C-A

44229988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76939472-T-C

44230000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76939460-C-G

44230000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76939460-C-T

http://identifiers.org/hco/13/GRCh38#44230189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76939050-C-A

44230553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76938724-T-C

44230562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76938710-C-G

44231592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76937117-T-C

44231677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76937041-G-A

44231928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76936781-C-T

44232206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76936514-G-C

44232239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76936481-A-G

44232262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76936459-G-A

44232262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76936459-G-T

44232291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76936429-T-G

44232417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76936305-G-A

44232815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76935892-G-A

44233103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76935603-T-C

44233174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76935542-A-G

44233266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76935464-C-T

44233391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76935341-T-A

44233525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76935224-A-G

44235213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76934658-A-G

44235216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76934655-G-A

http://identifiers.org/hco/13/GRCh38#44235228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76934644-C-A

44235250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76934627-A-G

http://identifiers.org/hco/13/GRCh38#44235310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76934568-C-A

44235388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76934514-T-C

44235473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76934429-T-A

http://identifiers.org/hco/13/GRCh38#44235547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76934355-C-A

44235547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76934355-C-T

44235905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76933997-A-G

http://identifiers.org/hco/13/GRCh38#44235915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76933987-C-A

44236519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76933056-T-C

44236519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76933056-T-G

44236725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76932879-T-C

http://identifiers.org/hco/13/GRCh38#44236810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76932770-C-A

http://identifiers.org/hco/13/GRCh38#44236811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76932769-C-A

44237189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76931918-C-T

44237218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76931899-T-C

44237330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76931794-T-C

44237374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76931763-A-G

44237431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76931706-C-T

44237519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76931618-A-G

44238041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76931095-G-A

44238110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76931027-A-G

44238425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930716-G-A

http://identifiers.org/hco/13/GRCh38#44238529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76930604-C-A

44238649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930282-C-T

44238672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930259-G-A

44238787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930159-G-A

http://identifiers.org/hco/13/GRCh38#44238814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76930134-C-A

44238829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 76930119-T-A

44238929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76930032-T-A

44239120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929849-C-G

44239120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929849-C-T

http://identifiers.org/hco/13/GRCh38#44239167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76929804-C-A

44239167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929804-C-T

44239180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929791-G-A

44239248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929700-T-C

44239257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929691-G-A

44239301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929615-G-T

http://identifiers.org/hco/13/GRCh38#44239393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76929547-C-A

44239393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929547-C-T

http://identifiers.org/hco/13/GRCh38#44239553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#76929436-C-A

44239553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76929436-C-G

44240346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42674
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76928753-T-C