108894682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58436820-A-G

http://identifiers.org/hco/2/GRCh38#108894834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58436948-C-A

108894890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437006-G-A

http://identifiers.org/hco/2/GRCh38#108894891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58437007-C-A

108894891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437007-C-G

http://identifiers.org/hco/2/GRCh38#108894893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58437009-C-A

108894963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437067-G-T

http://identifiers.org/hco/2/GRCh38#108894981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58437085-C-A

http://identifiers.org/hco/2/GRCh38#108895017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58437121-C-A

108895017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437121-C-T

108895020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437124-A-G

108895115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437205-G-A

108895116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437206-G-T

108895327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437436-A-G

108895457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437574-A-G

http://identifiers.org/hco/2/GRCh38#108895543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58437651-A-C

108895622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437722-T-C

108895646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437757-T-C

108895646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437757-T-G

108895653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437764-C-T

108895700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437810-T-C

108895719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437828-G-A

108895719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437828-G-T

108895763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437867-C-T

108895842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437938-T-G

108895860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58437950-T-C

108896018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438070-C-T

108896025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438077-G-A

108896025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438077-G-T

108896169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438121-G-T

108896176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438128-A-G

108896225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438175-G-T

http://identifiers.org/hco/2/GRCh38#108896301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58438246-C-A

http://identifiers.org/hco/2/GRCh38#108896379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58438325-C-A

108896379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438325-C-G

108896379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438325-C-T

108896568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438499-T-C

108896574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438505-T-C

108896815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438589-G-A

108896815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438589-G-T

http://identifiers.org/hco/2/GRCh38#108896851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58438625-A-C

108896873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438651-C-G

108896873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438651-C-T

108896883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438662-G-A

108896883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 58438662-G-C

108896913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58438690-T-C

108897075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58438852-G-A

108897075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, missense_variant
orthologous variants: 58438852-G-T

108897120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58438897-G-A

108897298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58439083-T-C

108904779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58439881-G-A

108905035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58440100-G-C

108905129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58440323-G-A

108905207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58440474-G-A

108905574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58440857-C-T

108905780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441052-T-C

108905963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441242-A-G

108906037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441364-C-T

108906121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441486-G-A

108906203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441568-G-T

108906232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441597-G-A

108906232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441597-G-T

108906265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441678-G-A

108906265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441678-G-T

108906268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441681-G-T

108906274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441715-G-T

108906280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441733-C-T

108906425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441979-G-A

108906425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58441979-G-T

108906568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58442112-T-C

108906568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58442112-T-G

108906648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58442174-T-A

108906946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58442394-G-A

108907031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58442465-C-T

108907749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443058-G-T

108907751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443060-G-T

108907809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443113-T-C

108907881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58443183-G-A

108908013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58443315-G-A

108908013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, missense_variant
orthologous variants: 58443315-G-T

108908029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443331-C-T

108908118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443399-A-G

108908147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443428-G-A

108908147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443428-G-T

http://identifiers.org/hco/2/GRCh38#108908152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58443433-C-A

108908152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443433-C-G

108908161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443440-T-C

108908182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443461-A-G

http://identifiers.org/hco/2/GRCh38#108908278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58443563-C-A

108908372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443664-T-G

108908408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443699-G-T

108908640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58443898-C-T

108909315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58444667-G-A

108909402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58444769-T-G

108909566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58444979-G-A

http://identifiers.org/hco/2/GRCh38#108909575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58444988-C-A

108909575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58444988-C-T

108909628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445013-G-A

http://identifiers.org/hco/2/GRCh38#108909632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58445017-A-C

108909632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445017-A-T

108909744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445102-C-T

108909838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445189-C-T

108909867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445224-C-T

108909907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445264-C-T

108909965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445289-C-T

108910224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445464-G-A

108910399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445656-C-T

108910410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445668-A-G

108910448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445735-G-C

108910519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, missense_variant
orthologous variants: 58445819-C-T

108910547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445843-G-A

108910547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445843-G-T

108910564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445860-G-T

108910585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445878-T-A

108910585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445878-T-C

108910607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445901-T-A

108910656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445947-G-A

108910656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445947-G-T

108910665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445956-G-T

108910694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58445998-G-T

http://identifiers.org/hco/2/GRCh38#108910821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58446141-C-A

108910821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, missense_variant
orthologous variants: 58446141-C-G

108910821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, missense_variant
orthologous variants: 58446141-C-T

108910876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58446206-G-A

108910906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58446233-A-G

108911207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58446489-G-T

http://identifiers.org/hco/2/GRCh38#108911286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58446579-A-C

108911703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58446983-C-T

108911984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447207-C-T

108912094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447295-G-A

108912507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447633-A-T

http://identifiers.org/hco/2/GRCh38#108912582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58447701-C-A

108912582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447701-C-T

108912600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447714-T-A

108912600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447714-T-C

108912607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447721-C-T

http://identifiers.org/hco/2/GRCh38#108912718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58447819-C-A

108912718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58447819-C-T

108912736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58447837-G-A

108912736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58447837-G-T

http://identifiers.org/hco/2/GRCh38#108912787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58447888-C-A

108912787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447888-C-G

108912787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58447888-C-T

108916002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58450220-C-T

108916003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58450221-T-A

108916277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58450500-T-C

108916593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58450815-C-T

108916705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58450898-G-A

108916753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58450935-C-T

108916862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451052-C-T

108917759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451588-C-G

108917935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451762-G-T

108918049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451873-T-C

108918053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451876-C-T

108918108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451947-C-T

108918110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58451949-G-A

108918346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58452229-C-G

http://identifiers.org/hco/2/GRCh38#108918558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58452356-C-A

108919061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58452822-G-A

108920935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454167-G-A

108921047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454262-G-A

108921065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454286-C-G

http://identifiers.org/hco/2/GRCh38#108921074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58454295-C-A

108921074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454295-C-G

108921074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454295-C-T

108921225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454379-G-A

108921431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454561-G-A

108921578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454663-G-A

108921744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58454776-C-G

108922587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58455471-A-G

http://identifiers.org/hco/2/GRCh38#108922967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58455807-C-A

108923387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 58457154-T-A

108923591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457358-G-A

108923591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457358-G-T

108923597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457368-T-C

http://identifiers.org/hco/2/GRCh38#108923598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58457369-C-A

108923675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457448-C-G

108923678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457451-T-C

108923745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457611-T-A

108923803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457667-G-T

108924121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58457922-C-G

108924302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458026-C-T

108924322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458037-C-T

108924324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458039-C-T

http://identifiers.org/hco/2/GRCh38#108924325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58458040-C-A

108924421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458117-C-T

108924532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458231-A-G

108924615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458317-G-A

108924625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458327-G-A

108924625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458327-G-T

108924836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458580-T-A

108924840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458584-T-C

108924840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458584-T-G

108924869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458626-G-A

108925211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458761-T-C

108925293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58458869-G-A

108925482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58459071-G-A

108926380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58460613-T-G

108926591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58460846-C-T

108926930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461177-T-C

108926993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461257-T-C

108926993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461257-T-G

108927126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461372-C-G

108927299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461514-G-A

http://identifiers.org/hco/2/GRCh38#108927398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58461601-C-A

108927412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461615-G-A

108927524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58461714-G-A

http://identifiers.org/hco/2/GRCh38#108927654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58461908-A-C

108927736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58462063-G-T

108927811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58462143-C-T

http://identifiers.org/hco/2/GRCh38#108927853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58462185-C-A

108927871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58462203-A-T

108927875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58462207-A-G

108927875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58462207-A-T

http://identifiers.org/hco/2/GRCh38#108928163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58462542-A-C

108928629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58463720-G-A

108928630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58463721-G-C

http://identifiers.org/hco/2/GRCh38#108928883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58463992-C-A

108928883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58463992-C-G

http://identifiers.org/hco/2/GRCh38#108928925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58464020-A-C

108929056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464158-G-T

108929087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464188-G-A

108929087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464188-G-T

108929111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464212-A-G

http://identifiers.org/hco/2/GRCh38#108929113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58464215-C-A

108929113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464215-C-T

108929132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464234-G-T

http://identifiers.org/hco/2/GRCh38#108929141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58464243-C-A

108929141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464243-C-G

108929141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464243-C-T

108929142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464244-C-T

108929181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464260-G-A

108929181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464260-G-T

108929254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58464338-G-A

108929254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58464338-G-C

108929287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58464371-A-T

108929386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58464470-A-G

108929400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464479-G-A

108929400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464479-G-C

108929415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464490-T-A

108929415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464490-T-C

108929415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464490-T-G

108929455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58464519-G-T

http://identifiers.org/hco/2/GRCh38#108930011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58465090-A-C

108930011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465090-A-G

108930011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465090-A-T

http://identifiers.org/hco/2/GRCh38#108930061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58465142-C-A

108930061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465142-C-T

108930266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465331-G-A

108930274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465339-T-C

108930335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465376-C-T

108930356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58465381-G-A

108931000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58465922-C-G

108931030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 58465952-C-T

108931123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466024-G-A

108931123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466024-G-T

108931166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466081-A-G

108931497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466502-C-T

108931518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466513-T-C

http://identifiers.org/hco/2/GRCh38#108931562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58466574-A-C

108931750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466749-C-T

108931751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466750-A-T

108931752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58466751-C-T

http://identifiers.org/hco/2/GRCh38#108932056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58467038-C-A

108932242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58467220-G-T

108932252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58467230-A-G

108933207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58467732-G-T

108933382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58467892-C-T

108933540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468050-G-A

108933782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468213-G-A

108933969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468486-G-A

108934034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468550-G-A

108934034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468550-G-C

108934207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468702-T-A

108934207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58468702-T-C

108935379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58471508-T-C

http://identifiers.org/hco/2/GRCh38#108935490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58471613-C-A

108936022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58471988-G-A

108936133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472067-T-C

108936146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472091-C-T

108936230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472170-G-T

108936269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472201-G-A

108936373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472369-G-A

108936455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472449-G-A

108936707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58472680-G-A

108939518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474431-A-T

108939693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474567-C-T

108939699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474573-T-C

108939855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474722-G-T

108939930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474784-C-T

108939972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474797-C-T

108939973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474798-T-C

108939977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58474802-C-T

108940392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475031-G-A

108940469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475091-C-T

108940470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475092-T-C

108940682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475264-G-A

108940694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475276-C-T

108940737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475318-C-G

108940853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58475432-A-G

http://identifiers.org/hco/2/GRCh38#108941615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58476321-C-A

108941615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476321-C-T

108941621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476327-C-T

108941631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476337-G-A

108941743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476443-G-A

108941747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476444-A-G

108941907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476572-T-A

108942015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476642-G-A

108942289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476901-G-A

108942289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58476901-G-T

108942521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477107-G-A

http://identifiers.org/hco/2/GRCh38#108942526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58477112-C-A

108942613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477200-T-C

108942614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477201-G-A

108942644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477232-C-T

http://identifiers.org/hco/2/GRCh38#108942672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58477259-C-A

108942801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477360-C-T

108942863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477425-G-A

108943018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58477548-G-C

108943658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58478595-C-T

108943667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58478604-G-C

108943677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58478614-T-A

108943677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58478614-T-C

108944643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58479005-G-A

108944643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58479005-G-T

108944791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58479147-A-G

108944870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, undefined
orthologous variants: 58479192-C-T

108945117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58479385-G-A

108945608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58479821-G-A

108945686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58479884-C-T

http://identifiers.org/hco/2/GRCh38#108945692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58479890-A-C

http://identifiers.org/hco/2/GRCh38#108945704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58479902-C-A

108945896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58480010-G-A

108946104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58480209-A-G

108946107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58480212-C-T

108949643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481285-T-C

108949660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481302-G-A

108949742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481382-C-T

108949831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481443-A-G

108949876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481487-A-G

108949916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481526-G-A

108949940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58481548-T-G

108951019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58483762-G-A

108951088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58483827-C-T

108951115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58483853-G-A

108951244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58483919-G-A

108951395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484067-T-A

108951395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484067-T-C

108951424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484081-G-A

108951449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484103-C-T

108951455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484109-G-A

108951592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484262-G-A

108951718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484379-G-A

108951718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484379-G-C

108951755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484415-G-T

108951828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58484483-C-G

108952351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58485169-T-C

108952465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58485305-T-C

http://identifiers.org/hco/2/GRCh38#108952615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58485421-A-C

http://identifiers.org/hco/2/GRCh38#108957298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58487173-C-A

108957298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58487173-C-T

108957723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58487600-G-A

108958648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58488438-G-A

108959083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58488799-T-A

108959140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58488858-G-A

108962763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490236-C-T

108962906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490372-G-T

108962949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490414-G-A

108963044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490507-G-T

108963299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490765-T-C

108963308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490774-T-C

http://identifiers.org/hco/2/GRCh38#108963396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58490836-C-A

108963396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490836-C-T

108963397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490837-G-A

108963434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58490874-G-A

108963790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58491204-C-T

108964104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58491714-A-T

108964410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58491990-G-A

108964410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58491990-G-T

108964415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58491993-G-T

108964437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58492011-C-T

108965004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58492703-T-C

108965007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58492706-C-G

108965180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58492827-T-C

http://identifiers.org/hco/2/GRCh38#108965670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58493019-C-A

108965672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58493021-G-A

108965672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58493021-G-C

108965772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58493114-G-A

108965929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58493263-T-C

108966204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58493547-T-C

108967311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58495189-A-G

108967620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58495511-G-C

108967652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58495543-T-G

http://identifiers.org/hco/2/GRCh38#108967677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58495568-A-C

108967752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58495671-A-G

108968170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58496096-A-G

108968170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58496096-A-T

108968304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58496232-T-C

http://identifiers.org/hco/2/GRCh38#108968334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58496262-C-A

108968938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58496700-T-C

108971581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58498969-G-A

108971620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58499004-G-C

108971853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58499193-A-G

108971919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58499265-G-C

108972007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, undefined
orthologous variants: 58499356-C-T

108972118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58499462-C-T

108972337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, undefined
orthologous variants: 58499698-C-T

108974929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501439-G-C

108974929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501439-G-T

http://identifiers.org/hco/2/GRCh38#108975007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58501517-C-A

108975030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501536-C-T

108975183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501615-G-T

108975221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501653-G-A

108975307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501722-T-C

108975327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501742-G-T

108975377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58501788-C-T

108980271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58502144-C-G

108980512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58502376-A-T

108980585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58502438-T-C

108980795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58503017-G-C

http://identifiers.org/hco/2/GRCh38#108981485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58503818-C-A

108981485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58503818-C-T

http://identifiers.org/hco/2/GRCh38#108981494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58503827-C-A

108981494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58503827-C-T

108981495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58503828-T-C

108981495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58503828-T-G

108981502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58503835-C-T

108981937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58504156-T-C

http://identifiers.org/hco/2/GRCh38#108982594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#58504786-C-A

108982764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58504957-G-C

108982790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58504985-A-G

108982820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron_variant, undefined
orthologous variants: 58505013-G-T

108983031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58505146-T-C

108983186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58505278-C-T

108983192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58505284-C-T

108983238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58505362-C-T

108984959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: -T-C

108985970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58507911-T-C

108986028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58507967-G-A

108986073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508012-G-A

108986123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508070-G-A

108986376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508351-A-T

108986519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508457-T-C

108986715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508660-T-A

108986715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508660-T-G

108986791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58508931-T-C

108987269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58509412-C-G

108987271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58509414-G-C

108987334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58509476-G-C

108987357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58509499-G-A

108987713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510135-C-T

108987803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510205-C-T

108987918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510278-A-G

108988068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510431-G-T

108988096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510468-A-G

108988125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510499-C-T

108988222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510603-C-T

108988313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510668-A-T

108988354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510710-G-A

108988439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510789-T-C

108988499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510836-G-T

108988589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58510924-G-A

108988682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58511002-T-C

108988730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: intron variant
orthologous variants: 58511040-T-A

http://identifiers.org/hco/2/GRCh38#108989206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58511511-C-A

108989239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511541-G-A

108989244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511546-G-A

108989244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511546-G-T

http://identifiers.org/hco/2/GRCh38#108989245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58511547-C-A

http://identifiers.org/hco/2/GRCh38#108989262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58511564-C-A

108989265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511567-A-G

108989266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511568-C-T

108989344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511642-G-A

108989344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2895
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 58511642-G-T