100273126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38832510-C-T

100273148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832531-G-T

http://identifiers.org/hco/2/GRCh38#100273162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38832545-C-A

100273217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832583-A-G

100273217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832583-A-T

100273270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832632-G-A

100273402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832746-A-G

100273461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832804-A-G

100273534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832879-A-G

100273600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38832948-A-T

http://identifiers.org/hco/2/GRCh38#100273778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38833088-C-A

100273834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38833156-A-G

100282178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38835546-G-T

100282261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38835615-A-G

100282429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38835752-C-T

100282442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38835765-G-T

100282786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38835988-T-C

100282892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836049-G-T

100283013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836168-T-C

http://identifiers.org/hco/2/GRCh38#100283502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38836369-C-A

100283502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836369-C-G

100283730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836597-A-G

100283835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38836685-G-A

100283835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38836685-G-T

100283916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836747-A-T

100283921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836752-T-A

100283921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836752-T-G

http://identifiers.org/hco/2/GRCh38#100283936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#38836767-A-C

100283936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38836767-A-G

100283936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38836767-A-T

http://identifiers.org/hco/2/GRCh38#100283977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38836801-A-C

100283977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836801-A-G

100283977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836801-A-T

100284023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38836845-G-T

http://identifiers.org/hco/2/GRCh38#100284049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38836871-C-A

http://identifiers.org/hco/2/GRCh38#100284085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38836904-C-A

100284104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836923-T-A

100284104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3 prime UTR variant
orthologous variants: 38836923-T-C

http://identifiers.org/hco/2/GRCh38#100284160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#38836975-C-A

100284160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38836975-C-T

100284218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 38837031-C-T

100284547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: 38837358-C-G

100284547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: 38837358-C-T

http://identifiers.org/hco/2/GRCh38#100284552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#38837363-C-A

100284552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: 38837363-C-T

100284657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837461-T-A

100284669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837478-C-T

100284776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837571-A-T

100284778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837573-A-G

100284876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837667-T-A

100284888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837679-G-A

100284946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837759-T-C

100285012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837850-T-C

100285054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837896-C-T

100285085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38837926-A-T

100285539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38838373-A-G

100285890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38838733-A-T

http://identifiers.org/hco/2/GRCh38#100286766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38839593-C-A

100286766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839593-C-T

100286787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839614-T-C

100286788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839615-G-A

100286788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839615-G-T

100286828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839644-A-G

http://identifiers.org/hco/2/GRCh38#100286873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38839691-C-A

100286873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839691-C-T

100286888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839706-T-C

100287122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839940-T-C

100287152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839966-T-C

100287152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839966-T-G

100287153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38839967-T-G

100287338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840139-T-C

100287372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840171-G-A

100287443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840250-G-C

100287580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840493-T-C

http://identifiers.org/hco/2/GRCh38#100287592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38840505-C-A

100287592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840505-C-T

100287593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840506-G-A

100287813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840693-C-T

100287894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840751-T-C

100287934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840791-A-T

100287982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840826-A-G

http://identifiers.org/hco/2/GRCh38#100287993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38840837-A-C

100288010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38840853-A-T

100288249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38841081-C-T

100288323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38841150-C-T

100288393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38841215-C-T

100290200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38843280-T-C

100290467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38843527-G-T

100290503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38843558-A-G

http://identifiers.org/hco/2/GRCh38#100290527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38843587-C-A

100290527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38843587-C-T

100290616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38843668-T-C

100291551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38843899-C-T

100291777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844025-T-G

100291862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844102-G-A

100291862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844102-G-T

100291869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844109-C-T

100291891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844125-C-T

100292027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844246-G-T

100292105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844316-T-C

100292288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844486-G-A

100292362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844563-A-T

100292402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844600-T-A

100292403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38844601-A-T

http://identifiers.org/hco/2/GRCh38#100292419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38844612-C-A

100292864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845006-G-A

http://identifiers.org/hco/2/GRCh38#100292876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38845018-C-A

100292876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845018-C-G

100292877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845019-C-T

100293334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845407-G-A

100293334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845407-G-T

100293545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845623-A-T

100293583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845664-A-G

100293607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845681-T-G

100293608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845682-G-A

100293621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845695-C-T

100293623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845697-C-T

100293691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38845764-T-C

http://identifiers.org/hco/2/GRCh38#100294079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38845959-A-C

http://identifiers.org/hco/2/GRCh38#100294121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38846002-C-A

100294121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846002-C-T

http://identifiers.org/hco/2/GRCh38#100294141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38846022-C-A

100294144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846025-G-T

100294146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846027-A-T

100294174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846076-T-C

100294180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846082-A-T

http://identifiers.org/hco/2/GRCh38#100294243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38846136-A-C

100294419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846312-G-A

100294747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846615-C-T

100294748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846616-T-C

http://identifiers.org/hco/2/GRCh38#100295314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38846864-C-A

100295314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846864-C-T

100295420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38846905-A-G

100295439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: synonymous variant
orthologous variants: 38846924-G-A

100295570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38847058-T-G

100295581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38847069-T-C

100295595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38847083-T-C

100295601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38847089-A-G

100297964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850078-A-T

100298157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850297-G-A

100298157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850297-G-C

100298553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850541-A-G

100298630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850614-T-C

100298697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850678-T-G

100298812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850779-C-T

100298975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850939-C-G

100298975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850939-C-T

100298994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850958-A-G

http://identifiers.org/hco/2/GRCh38#100299034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38850998-C-A

100299034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850998-C-G

100299034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38850998-C-T

http://identifiers.org/hco/2/GRCh38#100299041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38851005-C-A

100299041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38851005-C-T

100299104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38851068-T-C

100299234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38851633-G-C

100299237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38851636-G-A

100299291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38851687-A-G

100299298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, missense_variant
orthologous variants: 38851694-G-A

http://identifiers.org/hco/2/GRCh38#100299354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38851750-C-A

100299369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38851765-A-G

100299396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38851792-T-C

100299650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38852232-T-C

100299650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38852232-T-G

100299710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38852287-C-T

100299805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: synonymous variant
orthologous variants: 38852388-T-C

100299806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: missense variant
orthologous variants: 38852389-G-A

http://identifiers.org/hco/2/GRCh38#100299909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#38852492-C-A

100299910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: synonymous variant
orthologous variants: 38852493-A-T

100299944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38852525-C-T

100299952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38852533-T-C

100300536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38854990-C-G

100300536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38854990-C-T

100300660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: missense variant
orthologous variants: 38855062-T-A

100300689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: missense variant
orthologous variants: 38855103-C-T

100300796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38855210-T-C

100301213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38855550-G-A

100301271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38855583-G-A

100301292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38855604-G-C

100301609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38855892-G-A

100301916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38856162-T-C

100301916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38856162-T-G

100302207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38856453-T-C

100302573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38856794-C-G

100302680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38856924-A-G

100302705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38856949-T-C

100302823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38857045-T-C

http://identifiers.org/hco/2/GRCh38#100302830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38857052-C-A

100302830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38857052-C-T

100303087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38857309-T-C

100303095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38857317-T-A

100303192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38857380-T-G

http://identifiers.org/hco/2/GRCh38#100309096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860216-A-C

100309096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860216-A-G

100309103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860223-A-G

100309103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860223-A-T

http://identifiers.org/hco/2/GRCh38#100309110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860231-A-C

100309110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: synonymous variant
orthologous variants: 38860231-A-G

100309267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860378-T-C

http://identifiers.org/hco/2/GRCh38#100309348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860417-A-C

100309348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860417-A-G

100309348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860417-A-T

http://identifiers.org/hco/2/GRCh38#100309353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860422-A-C

100309353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860422-A-G

100309353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860422-A-T

http://identifiers.org/hco/2/GRCh38#100309370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860438-A-C

http://identifiers.org/hco/2/GRCh38#100309384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860452-C-A

100309384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860452-C-T

100309389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860457-T-C

100309424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860492-A-G

http://identifiers.org/hco/2/GRCh38#100309444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860512-C-A

100309447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860515-G-A

100309447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860515-G-C

100309447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38860515-G-T

100309500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38860568-G-A

100309500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38860568-G-T

http://identifiers.org/hco/2/GRCh38#100309504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860572-C-A

http://identifiers.org/hco/2/GRCh38#100309543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38860608-A-C

100311951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38865278-A-G

100312074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38865353-A-G

100312220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38865455-T-C

100312585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38865668-C-T

100312609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38865692-A-T

100312687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38865724-C-T

100312959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38865900-G-A

100313078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38866011-C-T

100313087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: 38866020-G-T

http://identifiers.org/hco/2/GRCh38#100313100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38866030-A-C

http://identifiers.org/hco/2/GRCh38#100313112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38866046-C-A

100321392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: 38874829-G-A

100321392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: 38874829-G-C

100321392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: intron_variant, undefined
orthologous variants: 38874829-G-T

100321579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 38875016-G-A

100321579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 38875016-G-T

http://identifiers.org/hco/2/GRCh38#100321644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38875081-C-A

100321644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 38875081-C-T

http://identifiers.org/hco/2/GRCh38#100321653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#38875090-C-A

100321653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 38875090-C-G

100321653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 38875090-C-T

http://identifiers.org/hco/2/GRCh38#100321818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#38875240-C-A

100321818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 38875240-C-G

100321818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 38875240-C-T

http://identifiers.org/hco/2/GRCh38#100321974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38875396-C-A

100321974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 38875396-C-T

http://identifiers.org/hco/2/GRCh38#100321986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38875408-C-A

100321986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 38875408-C-G

100321986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 38875408-C-T

100322018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 38875440-G-A

100322018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 38875440-G-C

100322018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 38875440-G-T

100322226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5 prime UTR variant
orthologous variants: 38875592-G-A

100322226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5 prime UTR variant
orthologous variants: 38875592-G-T

100322254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38875620-G-A

100322254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38875620-G-C

100322284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5 prime UTR variant
orthologous variants: 38875638-G-T

http://identifiers.org/hco/2/GRCh38#100322346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#38875675-C-A

100322346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5 prime UTR variant
orthologous variants: 38875675-C-T

100322478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38875794-T-A

100322478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38875794-T-C

100322478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24788
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38875794-T-G