64280018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 83427003-C-T

64280041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 83427026-G-T

64280138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 83427127-C-G

64280138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 83427127-C-T

64280202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 83427191-A-G

64280211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427200-A-G

64280298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427294-T-G

64280319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427315-A-G

64280816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427677-A-G

64280967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427815-T-A

64280967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427815-T-C

64281001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427849-G-A

64281001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427849-G-C

64281001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427849-G-T

http://identifiers.org/hco/4/GRCh38#64281002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83427850-C-A

64281002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427850-C-G

64281002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427850-C-T

64281132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427983-G-C

64281147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427998-G-A

64281147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83427998-G-T

64281179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428031-T-C

64281427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428312-G-C

64281427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428312-G-T

64281428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428313-T-C

64281455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428339-A-G

64281455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428339-A-T

64281456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428340-C-T

64281457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428341-A-G

64281588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428470-G-A

64281588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428470-G-T

64281591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428473-G-A

64281591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428473-G-T

64281594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428476-A-G

64281623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428487-T-A

64281629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428493-A-T

http://identifiers.org/hco/4/GRCh38#64281649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83428513-A-C

64281652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428516-G-A

64281652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428516-G-T

64281899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428760-T-A

64281990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428843-A-T

64282006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428857-G-A

64282006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428857-G-T

64282104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83428950-A-T

http://identifiers.org/hco/4/GRCh38#64282210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83429057-C-A

64282210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83429057-C-T

http://identifiers.org/hco/4/GRCh38#64282231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83429077-A-C

64282231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83429077-A-G

64282366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83429211-C-T

64282441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83429284-T-C

64282477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83429322-T-C

http://identifiers.org/hco/4/GRCh38#64289732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83432090-C-A

64289732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense variant
orthologous variants: 83432090-C-G

64289732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense variant
orthologous variants: 83432090-C-T

64289821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83432155-A-G

64290029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83432256-T-G

64290122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83432367-G-A

http://identifiers.org/hco/4/GRCh38#64295795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83433641-C-A

http://identifiers.org/hco/4/GRCh38#64295796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83433642-A-C

64295796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83433642-A-G

64295872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83433701-T-G

64296044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83433881-A-G

64296071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83433910-T-C

64296323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83434102-C-G

64296451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83434218-A-T

http://identifiers.org/hco/4/GRCh38#64296485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83434252-A-C

64296905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83434623-T-C

64297193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83434880-G-A

64297359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435051-A-T

64297746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435406-G-C

64297819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435481-T-C

64297839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435501-C-T

64297882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435651-T-A

64298338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435946-T-C

64298338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83435946-T-G

64298426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83436009-A-G

64298465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83436054-T-A

64298489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83436066-G-A

64298489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: 83436066-G-T

http://identifiers.org/hco/4/GRCh38#64298820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83436388-A-C

64299081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83436600-T-C

64299521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83436955-A-G

64299685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437320-G-T

64299713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437344-G-C

64299881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437757-A-G

64299883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437759-T-C

64299888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437764-A-T

http://identifiers.org/hco/4/GRCh38#64299930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83437793-C-A

64299930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437793-C-T

64299985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83437846-T-C

64299985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83437846-T-G

64300041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437906-T-C

http://identifiers.org/hco/4/GRCh38#64300052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83437917-C-A

64300052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437917-C-G

64300052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437917-C-T

64300062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437926-G-A

64300062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437926-G-T

64300073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437940-T-C

64300090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437957-G-A

64300090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437957-G-C

64300090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437957-G-T

64300093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437959-A-G

64300093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437959-A-T

64300112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437979-T-C

64300112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437979-T-G

http://identifiers.org/hco/4/GRCh38#64300114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83437981-C-A

64300114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83437981-C-T

http://identifiers.org/hco/4/GRCh38#64300157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83438023-A-C

64300157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83438023-A-T

64300207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83438082-G-T

64304969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438898-G-A

64304969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438898-G-T

64304998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438919-G-C

64304998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438919-G-T

64305026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438948-A-G

http://identifiers.org/hco/4/GRCh38#64305050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83438971-A-C

64305050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438971-A-G

64305051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438972-G-A

64305051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438972-G-C

64305051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83438972-G-T

64305156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83439077-C-T

64309892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83442487-G-A

64309894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83442489-A-G

http://identifiers.org/hco/4/GRCh38#64309923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83442518-C-A

64309923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83442518-C-T

64310079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83442890-T-A

64310079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83442890-T-C

64310087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83442904-T-A

64310188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443001-A-G

64310194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443007-A-G

64310218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443029-G-A

64310312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443124-G-T

64310334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443146-T-C

64310357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443169-T-C

64310365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443177-T-C

64310454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443264-G-A

64310454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443264-G-T

64310511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83443319-G-T

64312414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83446651-T-C

64313207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83447483-T-C

http://identifiers.org/hco/4/GRCh38#64313233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83447504-C-A

64313250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83447518-T-A

64314637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83448686-G-A

64314637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83448686-G-C

64314637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83448686-G-T

http://identifiers.org/hco/4/GRCh38#64314641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83448690-C-A

http://identifiers.org/hco/4/GRCh38#64314676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83448725-C-A

64314676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83448725-C-T

64314853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83448907-T-C

64314853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83448907-T-G

64314876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83448940-G-T

64316098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450390-T-C

64316124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450416-A-G

64316363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450657-A-G

http://identifiers.org/hco/4/GRCh38#64316492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83450800-A-C

64316492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450800-A-G

64316555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450860-A-G

64316564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450869-A-G

64316588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83450891-T-C

http://identifiers.org/hco/4/GRCh38#64316648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83450957-A-C

64316794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451087-C-T

64316935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451229-T-A

64316935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451229-T-C

http://identifiers.org/hco/4/GRCh38#64316944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83451238-C-A

64316966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451278-A-T

64317265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451583-C-T

http://identifiers.org/hco/4/GRCh38#64317293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83451611-A-C

64317490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451793-A-T

64317599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83451900-T-G

http://identifiers.org/hco/4/GRCh38#64317707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83452018-A-C

64317707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452018-A-G

64317738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452049-G-A

64317878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452238-C-T

64317890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452246-C-T

64318186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452547-C-G

64318186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452547-C-T

64318217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452577-T-C

64318269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83452631-C-T

64319565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454227-G-A

64319565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454227-G-C

64319565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454227-G-T

64319883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454487-T-A

64319983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454580-C-T

64320173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454759-T-C

http://identifiers.org/hco/4/GRCh38#64320174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83454760-C-A

64320309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454892-A-T

64320316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83454899-A-G

http://identifiers.org/hco/4/GRCh38#64320458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83455031-C-A

64320464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455037-G-A

64320738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455310-G-A

64320885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455486-C-T

64320890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455491-C-G

64320952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455553-T-C

64321127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455665-C-T

64321341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83455978-G-A

64322661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457021-G-T

http://identifiers.org/hco/4/GRCh38#64322680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83457041-A-C

64322692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83457053-G-A

64322692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83457053-G-T

64322777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83457138-T-C

http://identifiers.org/hco/4/GRCh38#64322814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83457175-A-C

64322814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457175-A-G

64322846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457207-G-A

64322846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457207-G-T

64322864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457223-G-A

64322864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457223-G-T

64322898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457257-T-A

http://identifiers.org/hco/4/GRCh38#64322946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83457302-C-A

64322967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457322-A-G

64325489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83457477-T-G

64325928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83458723-T-C

64325976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83458769-A-T

64326048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83458833-C-T

http://identifiers.org/hco/4/GRCh38#64326058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83458843-C-A

http://identifiers.org/hco/4/GRCh38#64326570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83459309-C-A

64326627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83459354-G-A

http://identifiers.org/hco/4/GRCh38#64326692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83459409-C-A

64326692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83459409-C-T

64326781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83459495-C-T

64326852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83459552-C-G

64326952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83459728-C-T

64327078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83459981-A-G

64327447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83460331-A-G

64327804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83460639-A-G

64327857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83460674-C-T

64327963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83460786-T-G

64328051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83460871-A-G

64328405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461027-T-C

64328465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83461085-A-G

64328504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83461123-C-T

http://identifiers.org/hco/4/GRCh38#64328539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83461158-A-C

http://identifiers.org/hco/4/GRCh38#64328592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83461211-A-C

http://identifiers.org/hco/4/GRCh38#64372861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83483388-C-A

64375147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486071-A-G

64375264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486184-T-A

64375264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486184-T-C

64375368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486274-T-C

64375547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486449-T-A

64375578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486493-A-G

64375642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486551-G-A

http://identifiers.org/hco/4/GRCh38#64375882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83486754-A-C

64375988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83486927-A-G

http://identifiers.org/hco/4/GRCh38#64376084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83487024-A-C

64377569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83489479-C-T

64377610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83489513-T-A

http://identifiers.org/hco/4/GRCh38#64377844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83489725-C-A

64377934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83489820-T-C

64377984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83489868-G-A

64378001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83489885-T-C

64378549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83490734-T-G

64378606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83490791-C-T

64379071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83491394-G-T

64379094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83491419-T-C

64379199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83491535-G-A

http://identifiers.org/hco/4/GRCh38#64403932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83497985-C-A

64403932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83497985-C-G

http://identifiers.org/hco/4/GRCh38#64404013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83498040-A-C

64404261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83498261-G-A

64404378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83498370-C-G

64404415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83498407-G-A

64407918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501597-T-C

http://identifiers.org/hco/4/GRCh38#64407940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83501618-A-C

64407940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501618-A-G

64407943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501621-T-C

64408194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501844-C-T

64408227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501868-C-T

64408293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501924-T-C

64408309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83501943-A-G

http://identifiers.org/hco/4/GRCh38#64408863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83502440-A-C

http://identifiers.org/hco/4/GRCh38#64409172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#83502674-A-C

64409172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83502674-A-T

64409262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83502764-C-G

64409262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83502764-C-T

64409263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83502765-A-G

64409370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83502866-G-T

64409372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83502868-T-C

64409421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27365
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83502917-T-G