153992816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3 prime UTR variant
orthologous variants: 90119338-A-G

http://identifiers.org/hco/1/GRCh38#153992824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90119330-C-A

153992824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3 prime UTR variant
orthologous variants: 90119330-C-G

153992824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3 prime UTR variant
orthologous variants: 90119330-C-T

http://identifiers.org/hco/1/GRCh38#153992872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90119285-C-A

153992872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90119285-C-G

153992908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90119249-G-C

153992908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90119249-G-T

153992954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119205-G-A

153992984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119160-T-C

153992987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119157-T-C

http://identifiers.org/hco/1/GRCh38#153993030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#90119120-C-A

153993030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 90119120-C-G

153993030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 90119120-C-T

153993062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 90119088-T-G

153993085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 90119065-G-A

153993117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119034-G-T

http://identifiers.org/hco/1/GRCh38#153993120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90119031-A-C

153993120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119031-A-G

153993136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119002-T-A

153993136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90119002-T-C

153993148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90118990-G-T

153994714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117965-G-A

153994794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117923-A-T

http://identifiers.org/hco/1/GRCh38#153994795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90117922-C-A

153994795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117922-C-T

http://identifiers.org/hco/1/GRCh38#153995006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90117849-C-A

153995006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117849-C-T

153995010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117845-T-A

153995010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117845-T-C

153995010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117845-T-G

153995023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117817-A-G

153995055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117788-T-A

153995055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117788-T-C

153995141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, missense_variant
orthologous variants: 90117698-C-G

153995141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, missense_variant
orthologous variants: 90117698-C-T

153995191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117651-G-A

153995191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90117651-G-T

153996146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90116919-G-T

153996147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90116918-C-T

153996151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90116914-G-T

153996224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90116845-G-A

154000936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 90114712-A-G

154000963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 90114685-G-C

154000989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 90114659-A-T

154001172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90114511-G-A

154001172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90114511-G-T

154001197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90114486-T-A

154002140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90110905-C-G

154009791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90109498-T-A

154009791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90109498-T-C

154009875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90109427-A-T

http://identifiers.org/hco/1/GRCh38#154009901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90109408-C-A

154009901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90109408-C-T

154010110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90109233-G-A

154010110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90109233-G-C

154012184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90107286-G-C

154012184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90107286-G-T

154012358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90107116-C-G

154012358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90107116-C-T

154012406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90107075-T-A

154012506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90106996-T-G

154018845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90105574-C-T

154018989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90105436-G-T

http://identifiers.org/hco/1/GRCh38#154019157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90105275-C-A

154019165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90105267-C-T

http://identifiers.org/hco/1/GRCh38#154021772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90100891-C-A

http://identifiers.org/hco/1/GRCh38#154021978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90100573-C-A

154022210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90100393-C-T

154022331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: 90100272-C-T

154022355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90100248-C-T

154022887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90098564-G-A

154023008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90098447-G-T

154023101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90098354-C-T

154023114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90098341-T-A

154023114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90098341-T-C

154023298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: splice acceptor variant
orthologous variants: 90098157-C-T

154025207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90097237-C-T

http://identifiers.org/hco/1/GRCh38#154025537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90096905-C-A

154025636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90096806-A-G

154025636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90096806-A-T

154025708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90096734-G-C

154025740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90096702-G-C

154025740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90096702-G-T

154025753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90096689-G-T

http://identifiers.org/hco/1/GRCh38#154027467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90093459-C-A

154027467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90093459-C-T

154027563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90093371-C-T

154027637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90093288-A-G

154027679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90093243-G-A

154027679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90093243-G-T

154029946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, missense_variant
orthologous variants: 90092838-C-T

http://identifiers.org/hco/1/GRCh38#154029959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90092825-C-A

154029959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, missense_variant
orthologous variants: 90092825-C-G

154029960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, missense_variant
orthologous variants: 90092824-A-G

154044921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90090905-A-G

154046087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: 90089898-T-C

154046130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90089855-A-G

154046131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90089854-G-A

http://identifiers.org/hco/1/GRCh38#154046133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90089852-C-A

154046222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90089765-G-A

154046263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90089724-G-A

154046381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90089177-G-A

154054069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088978-A-T

154054190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088886-T-C

154054349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90088734-T-C

154054427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088656-T-C

http://identifiers.org/hco/1/GRCh38#154054434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90088649-C-A

154054434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088649-C-T

http://identifiers.org/hco/1/GRCh38#154054467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90088619-C-A

154054467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088619-C-G

http://identifiers.org/hco/1/GRCh38#154054472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90088614-C-A

http://identifiers.org/hco/1/GRCh38#154054523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90088572-C-A

154054523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088572-C-G

154054523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088572-C-T

154054527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088568-T-A

http://identifiers.org/hco/1/GRCh38#154054529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90088566-C-A

154054529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088566-C-T

154054596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088500-T-G

154054616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90088480-G-A

http://identifiers.org/hco/1/GRCh38#154054809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90087478-A-C

154056760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90083315-A-T

http://identifiers.org/hco/1/GRCh38#154056772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90083303-A-C

154056879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90083211-G-A

154056992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90083091-G-T

154057000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90083084-A-G

154057004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90083036-G-A

154057004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90083036-G-T

154057216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90082717-A-G

154057774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90082084-C-T

154057801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90082038-C-G

154057801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90082038-C-T

154057808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90082031-A-G

154057890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90081940-T-C

154057978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90081858-G-A

154057978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90081858-G-T

154058089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 90081762-G-A

154058089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 90081762-G-C

154058251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90081602-T-G

154058311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90081551-T-A

154058312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90081550-G-T

154058430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079626-G-A

154058436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079620-G-A

154058436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079620-G-T

154058470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079596-A-G

154058477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079589-C-G

154058477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079589-C-T

154058521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079549-A-G

154059568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90079267-A-G

154060508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90077995-A-G

154060508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90077995-A-T

http://identifiers.org/hco/1/GRCh38#154060510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90077993-C-A

154060510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90077993-C-T

154060726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90077786-G-T

154060970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90077371-G-T

154061012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90077329-T-C

154061022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90077319-C-T

http://identifiers.org/hco/1/GRCh38#154061557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90076715-A-C

154070298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: 90075206-A-G

154070319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: 90075185-C-T

http://identifiers.org/hco/1/GRCh38#154070482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90075022-A-C

154089401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90067328-G-C

154089401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90067328-G-T

154089437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90067292-T-C

154089467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90067262-G-A

http://identifiers.org/hco/1/GRCh38#154089649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90067084-C-A

154089649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90067084-C-T

154089974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066756-G-A

http://identifiers.org/hco/1/GRCh38#154090068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90066655-C-A

154090075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066633-T-C

154090134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066565-C-T

154090165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066534-G-A

154090182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066497-C-G

154090207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066472-T-A

154090207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066472-T-C

154090211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90066468-T-A

154094893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90062032-G-T

154094927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90062003-T-A

154094993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90061937-G-T

154097648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059970-T-A

154097735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059903-T-C

154099545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059332-A-G

154099545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059332-A-T

154099554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059323-T-C

154099561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059316-A-G

154099566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90059312-T-C

154100059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90058492-A-G

154100089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90058462-G-T

154100184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058367-T-C

154100187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058364-G-C

154100187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058364-G-T

154100221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058337-A-G

154100251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058317-A-T

154100447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058260-T-A

154100541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90058177-G-T

154100850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90057856-T-A

154100850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90057856-T-C

154100856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90057852-T-C

154102662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90052886-T-A

154102788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90052747-T-G

154103979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90051694-A-G

154103979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90051694-A-T

154104068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90051606-T-A

154104229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90051445-T-C

154115257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90048286-C-T

154115277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90048266-T-C

154115458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, undefined
orthologous variants: 90048111-A-T

154116793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90046540-C-T

154117899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044132-C-T

154117950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044080-G-A

154117950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044080-G-C

154117950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044080-G-T

154117962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044068-A-G

154117965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044065-G-A

154117965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90044065-G-T

http://identifiers.org/hco/1/GRCh38#154118012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90044016-A-C

154118661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90043501-G-C

154118749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: 90043413-A-G

154118941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90043232-T-C

154118941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90043232-T-G

154118943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90043230-A-T

154124605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90042451-G-A

154124858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90042301-A-G

154124889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90042269-C-T

154126265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90042061-A-G

154126265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90042061-A-T

154126348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90041983-G-A

154126387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90041944-A-G

http://identifiers.org/hco/1/GRCh38#154126695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90040396-A-C

154127392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: synonymous variant
orthologous variants: 90039650-T-C

154127399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90039643-C-T

154129269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90036496-T-C

154129269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90036496-T-G

http://identifiers.org/hco/1/GRCh38#154129402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90036362-C-A

154129402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90036362-C-G

154129402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90036362-C-T

154129439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90036332-A-G

154129471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90036297-T-C

http://identifiers.org/hco/1/GRCh38#154129634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90035564-C-A

154129634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90035564-C-T

154129716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90035426-G-A

154129764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90035380-G-A

154129847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90035313-A-G

154131291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90033439-G-A

154131291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90033439-G-T

http://identifiers.org/hco/1/GRCh38#154131316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90033414-A-C

154135718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031770-G-A

154135718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031770-G-T

http://identifiers.org/hco/1/GRCh38#154135719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90031769-C-A

154135719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031769-C-T

http://identifiers.org/hco/1/GRCh38#154135770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90031718-C-A

154135770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031718-C-G

154135777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031711-G-T

154136039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031445-T-C

154136109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031374-T-C

154136250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90031210-G-A

154137910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90030313-G-A

http://identifiers.org/hco/1/GRCh38#154137976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90030250-C-A

154137976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90030250-C-T

http://identifiers.org/hco/1/GRCh38#154137994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90030238-C-A

154137994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90030238-C-T

154138213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90030017-A-G

154138213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90030017-A-T

154139917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90027207-G-A

154139941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90027183-T-A

154139941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: missense variant
orthologous variants: 90027183-T-C

154139972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90027152-T-C

154140011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90027115-G-T

154141421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90025943-T-C

154142665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: -C-T

154142679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/1/GRCh38#154143394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90022545-C-A

154143403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022536-C-T

154143431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022506-T-C

154143598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022338-G-C

154143611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022321-A-G

154143612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022320-A-G

154143614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022318-A-G

154143629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022301-T-A

154143641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90022289-A-G

154145539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90020625-T-C

154152590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014650-G-A

154152590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014650-G-C

154152590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014650-G-T

154152673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014540-A-G

154152707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014450-G-T

http://identifiers.org/hco/1/GRCh38#154152802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90014274-C-A

154152802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 90014274-C-T

154152935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014143-A-G

154152972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014107-G-A

154152972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: 90014107-G-T

http://identifiers.org/hco/1/GRCh38#154152981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#90014098-A-C

154154975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 90011538-G-A

154155023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 90011493-A-G

154155023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29915
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 90011493-A-T