http://identifiers.org/hco/12/GRCh38#8032788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122796935-A-C

8032788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122796935-A-G

8032800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122796947-T-C

http://identifiers.org/hco/12/GRCh38#8032843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122796988-A-C

8032878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797024-T-C

8032937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797082-C-T

8032954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797096-A-G

http://identifiers.org/hco/12/GRCh38#8032956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122797098-A-C

8032956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797098-A-G

8033066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797196-G-A

8033066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797196-G-T

http://identifiers.org/hco/12/GRCh38#8033099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122797229-C-A

8033114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797244-A-G

http://identifiers.org/hco/12/GRCh38#8033236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122797333-C-A

8033236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797333-C-G

http://identifiers.org/hco/12/GRCh38#8033261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122797358-A-C

8033261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797358-A-G

8033318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797417-G-A

8033318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797417-G-T

8033470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797574-A-G

8033470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797574-A-T

8033496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797600-T-A

8033496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797600-T-C

8033496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797600-T-G

8033820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797916-A-G

8033821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5 prime UTR variant
orthologous variants: 122797917-A-G

8034178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 122798228-G-T

8034320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122798383-C-T

8034515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122798571-C-T

8034705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122798741-A-G

8034757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122798795-C-T

8035222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799267-T-C

8035318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799360-G-A

8035354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799399-C-T

8035416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799460-C-G

8035659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799705-A-G

8035848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799875-C-G

8035955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122799974-G-A

8036036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122800037-A-T

8036053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122800054-T-G

8036266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122800980-T-C

8036677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122801393-C-T

8037333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, undefined
orthologous variants: 122801705-T-C

8037540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122801902-C-T

http://identifiers.org/hco/12/GRCh38#8037604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122801961-C-A

8038005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122802544-G-A

8038318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122802836-G-A

http://identifiers.org/hco/12/GRCh38#8038334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122802863-A-C

8038338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122802867-G-A

8038583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122803133-A-G

8038900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122803465-T-C

8039084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, undefined
orthologous variants: 122803650-C-T

8039285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122804145-G-A

8039317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122804172-T-C

8039381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122804228-C-T

8039487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122804330-A-G

8039982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122805279-T-C

8040039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122805336-C-T

8040063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122805360-T-C

8040396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122805673-G-A

8040944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122806058-T-C

http://identifiers.org/hco/12/GRCh38#8041018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122806117-C-A

8041018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122806117-C-T

8041123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122806613-C-G

8042126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122807971-C-T

8042292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808067-A-G

8042513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808280-T-C

8042599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808336-T-G

http://identifiers.org/hco/12/GRCh38#8042619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122808356-C-A

8042619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808356-C-T

8042649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808386-C-T

http://identifiers.org/hco/12/GRCh38#8042654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122808391-C-A

8042654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122808391-C-G

8042726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 122808463-T-C

8042834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808557-T-A

8042834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808557-T-C

8042838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808561-G-A

8042838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808561-G-T

8042899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808624-C-T

8043120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808974-G-A

8043132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122808985-G-A

http://identifiers.org/hco/12/GRCh38#8043250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122809122-C-A

8043250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122809122-C-T

http://identifiers.org/hco/12/GRCh38#8043274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122809152-C-A

http://identifiers.org/hco/12/GRCh38#8043395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122809339-C-A

8043395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122809339-C-T

8043646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122809639-G-T

8043862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810027-T-C

http://identifiers.org/hco/12/GRCh38#8043939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122810108-C-A

8043978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122810147-G-A

8043978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122810147-G-T

8044040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122810209-G-A

http://identifiers.org/hco/12/GRCh38#8044116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122810290-C-A

8044116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810290-C-G

8044230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810400-G-A

8044230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810400-G-T

8044236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810412-A-G

8044243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810419-G-A

8044243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810419-G-T

8044258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810434-G-C

8044258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810434-G-T

8044613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810510-T-C

8044632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810529-T-C

8045022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810877-A-G

8045031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810886-T-C

http://identifiers.org/hco/12/GRCh38#8045067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122810914-A-C

http://identifiers.org/hco/12/GRCh38#8045078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122810925-C-A

8045078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810925-C-T

http://identifiers.org/hco/12/GRCh38#8045085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122810932-C-A

8045085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810932-C-G

8045085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122810932-C-T

8046174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122811535-G-C

8046174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122811535-G-T

8046448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122812175-C-T

8046552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122812283-T-C

8046643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122812372-T-C

8046889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122813803-G-A

8046990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122813911-A-G

8047071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122814396-A-G

8047102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122814427-C-T

8047768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122814676-A-T

8047845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122814742-T-G

8048024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122814904-G-A

http://identifiers.org/hco/12/GRCh38#8048075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122814955-C-A

8048075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122814955-C-T

8048117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122814997-A-G

8048123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122815003-G-A

8048123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122815003-G-T

8048144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122815024-C-T

http://identifiers.org/hco/12/GRCh38#8048216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122815096-C-A

8048218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122815098-A-G

8048218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122815098-A-T

8048377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815224-A-G

8048405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815259-T-C

8048425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815279-G-A

8048425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815279-G-T

http://identifiers.org/hco/12/GRCh38#8048568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122815450-C-A

8048692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122815538-T-C

8048773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122815619-C-T

8048782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122815628-G-A

8048782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122815628-G-C

http://identifiers.org/hco/12/GRCh38#8048815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122815669-C-A

8048815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815669-C-T

8048887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815718-A-G

8049022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815836-G-A

8049063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815879-G-C

8049070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122815886-G-A

8049222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816283-G-A

8049222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816283-G-T

8049284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816337-G-A

8049284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816337-G-T

8049312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816365-G-A

8049312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816365-G-C

8049312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816365-G-T

8049315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816368-G-A

8049315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816368-G-C

8049315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron variant
orthologous variants: 122816368-G-T

8049408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122816466-C-T

8049478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122816536-C-G

8049478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: 122816536-C-T

http://identifiers.org/hco/12/GRCh38#8049479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122816537-C-A

8049513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122816571-C-G

8049552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: synonymous variant
orthologous variants: 122816610-G-A

http://identifiers.org/hco/12/GRCh38#8049575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122816633-C-A

8049619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816672-G-A

8049658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816710-G-T

8049705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816752-A-G

8049712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816759-T-A

8049712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816759-T-C

8049762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816819-T-C

http://identifiers.org/hco/12/GRCh38#8049789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122816842-C-A

8049790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816843-A-G

8049799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816852-G-A

8049799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816852-G-T

8049809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816862-G-T

8049955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816968-G-C

8049955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122816968-G-T

http://identifiers.org/hco/12/GRCh38#8050345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122817016-C-A

8050345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122817016-C-G

8050345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122817016-C-T

8050380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122817050-C-T

8050389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122817059-T-A

8050389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122817059-T-C

8050400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122817070-C-T

http://identifiers.org/hco/12/GRCh38#8050495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122817158-C-A

8050495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122817158-C-T

8050508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122817171-T-C

8050532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122817195-T-C

8050532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122817195-T-G

http://identifiers.org/hco/12/GRCh38#8050586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122817249-C-A

http://identifiers.org/hco/12/GRCh38#8050772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122817437-C-A

8050772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122817437-C-G

8051474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122817854-A-G

8052557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122818377-G-A

http://identifiers.org/hco/12/GRCh38#8052596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122818404-C-A

8052692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122819653-C-G

http://identifiers.org/hco/12/GRCh38#8052697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122819658-C-A

8052781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122819742-G-T

8052866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122819823-G-T

http://identifiers.org/hco/12/GRCh38#8052925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122819882-C-A

8052925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122819882-C-T

http://identifiers.org/hco/12/GRCh38#8053025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122819978-C-A

8053195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820131-A-T

8053210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820146-A-G

8053210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820146-A-T

http://identifiers.org/hco/12/GRCh38#8053423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122820350-C-A

8053424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820351-T-C

8053424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820351-T-G

8053430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820357-C-T

http://identifiers.org/hco/12/GRCh38#8053434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122820361-C-A

8053494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820423-A-G

8053500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820429-G-A

8053500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820429-G-T

8053583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820485-G-A

8053583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820485-G-C

8053583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820485-G-T

8053886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122820761-A-G

http://identifiers.org/hco/12/GRCh38#8054042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122820916-C-A

8054193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821070-T-C

8054198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821075-G-A

8054198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821075-G-T

8054210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821086-G-A

8054210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821086-G-T

8054228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821105-A-G

8054336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821192-C-T

8054362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821223-T-C

8054389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821244-A-G

8054589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821425-G-A

8054589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821425-G-T

http://identifiers.org/hco/12/GRCh38#8054704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122821541-C-A

8054769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821603-G-A

8054769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821603-G-T

8054937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821761-T-C

8055083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821886-G-A

8055083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821886-G-T

http://identifiers.org/hco/12/GRCh38#8055086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122821889-C-A

8055099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821902-T-C

8055104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821907-C-G

http://identifiers.org/hco/12/GRCh38#8055105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#122821908-A-C

8055105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821908-A-G

8055125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821928-T-C

8055135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122821938-T-C

8055207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122822011-G-A

8055207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122822011-G-C

8055207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122822011-G-T

8055263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122822066-A-G

8055321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24818
most severe consequence: 3 prime UTR variant
orthologous variants: 122822122-T-G