106357928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: missense variant
orthologous variants: 84458379-G-A

http://identifiers.org/hco/12/GRCh38#106357968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84458419-C-A

106357968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458419-C-T

106358026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458477-C-T

http://identifiers.org/hco/12/GRCh38#106358029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84458480-C-A

106358029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458480-C-G

106358029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458480-C-T

106358053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458503-G-A

106358053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458503-G-T

106358065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458515-G-A

106358065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458515-G-C

106358065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458515-G-T

http://identifiers.org/hco/12/GRCh38#106358082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84458532-A-C

106358082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458532-A-G

106358085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458535-G-T

106358102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458550-C-G

106358102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458550-C-T

106358105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458553-T-C

106358105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458553-T-G

http://identifiers.org/hco/12/GRCh38#106358110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84458558-C-A

106358110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458558-C-T

106358111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458559-A-G

106358112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458560-G-A

106358112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458560-G-C

106358112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458560-G-T

106358121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458567-T-A

106358121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458567-T-C

106358121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458567-T-G

106358124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458570-G-C

http://identifiers.org/hco/12/GRCh38#106358129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84458575-C-A

106358129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458575-C-T

106358130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458576-G-A

106358130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458576-G-C

106358130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458576-G-T

106358165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458607-G-A

106358165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458607-G-C

106358165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458607-G-T

106358217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458658-G-C

106358217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84458658-G-T

106358220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 84458661-T-C

106358222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 84458663-G-T

106358248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458690-G-A

106358248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458690-G-T

106358309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458756-G-A

106358309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458756-G-T

106358337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458784-G-A

106358337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458784-G-T

106358409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458853-G-A

http://identifiers.org/hco/12/GRCh38#106358497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84458943-C-A

106358542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84458989-C-T

106358712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84459143-C-T

http://identifiers.org/hco/12/GRCh38#106358736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84459167-A-C

106363678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84463934-C-T

106363694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84463950-G-A

http://identifiers.org/hco/12/GRCh38#106363752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84463999-A-C

106363826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84464067-T-C

106363928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84464172-T-C

106366518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 84464349-G-A

106366566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 84464397-T-C

106366610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84464441-A-G

106366784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84464614-G-A

106367554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84465807-T-G

106367586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84465840-T-G

106367665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84465901-G-A

106368131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84466333-A-T

106368282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84466494-T-C

106368396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84466607-T-C

106369135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84467534-A-G

http://identifiers.org/hco/12/GRCh38#106369164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84467561-C-A

106369164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84467561-C-G

106369165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84467562-A-T

106369221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84467603-G-A

106369221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84467603-G-T

106369371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84467732-A-G

http://identifiers.org/hco/12/GRCh38#106369714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#84468450-C-A

106369714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468450-C-G

106369714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468450-C-T

http://identifiers.org/hco/12/GRCh38#106369726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#84468462-C-A

106369726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468462-C-T

106369757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468521-T-A

106369757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468521-T-C

106369757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468521-T-G

106369765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468529-G-A

106369765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, undefined
orthologous variants: 84468529-G-T

106369927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84468665-C-G

http://identifiers.org/hco/12/GRCh38#106370099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84468820-C-A

http://identifiers.org/hco/12/GRCh38#106376243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84470671-C-A

106376243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84470671-C-G

106376252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84470680-T-C

106376320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84470728-G-A

106376320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84470728-G-T

http://identifiers.org/hco/12/GRCh38#106376338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84470744-C-A

http://identifiers.org/hco/12/GRCh38#106376383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84470789-A-C

106376410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84470816-A-G

106376446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: missense variant
orthologous variants: 84470852-T-G

106376905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471040-A-G

106376943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471074-T-C

106376973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471092-C-G

106376973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471092-C-T

106377179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471292-A-G

106377379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471640-A-G

106377451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471708-A-G

106377678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471923-A-T

106377689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84471933-A-T

106378217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84473870-A-G

106378637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84474269-C-T

106378651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84474283-T-A

106378873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84474465-C-T

106379047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84474621-C-T

106379386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84474863-A-T

106379610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475066-G-A

106379632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475087-A-G

106379788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475334-T-A

106379931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475521-T-C

106379998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475573-G-A

106380012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475587-A-G

106380013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475588-A-G

106380028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 84475603-T-A

106380028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 84475603-T-C

106380079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84475654-A-G

106380189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84475764-T-G

106385529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477060-C-G

106385529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477060-C-T

106385672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477168-G-A

http://identifiers.org/hco/12/GRCh38#106385786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84477281-A-C

http://identifiers.org/hco/12/GRCh38#106385860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84477353-A-C

106385860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477353-A-G

106385965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477445-A-G

106386029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477490-A-G

106386113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477567-A-G

106386184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477578-A-G

106386373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477611-T-A

http://identifiers.org/hco/12/GRCh38#106386386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84477624-C-A

106386513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477744-A-G

106386543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84477764-A-G

http://identifiers.org/hco/12/GRCh38#106387040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84477958-C-A

106387259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478104-G-C

106387392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478205-A-G

106387392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478205-A-T

106387495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478253-A-G

106387495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478253-A-T

106387532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478289-G-T

106387714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478469-A-G

106387754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478508-A-G

106387782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478536-C-G

106387782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478536-C-T

106387967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478704-T-C

http://identifiers.org/hco/12/GRCh38#106388156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84478883-A-C

106388172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84478899-A-G

106389164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84479715-A-G

106389245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84479780-T-C

106389247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84479782-A-G

106389354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84479882-G-A

106389474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84479999-C-T

106390591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84480306-T-G

106390655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84480365-G-T

106390690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84480401-G-A

106390690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84480401-G-T

106391523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84481593-C-T

106391635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84481649-T-C

106391648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84481662-A-G

106391656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84481670-G-A

http://identifiers.org/hco/12/GRCh38#106391851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84481831-A-C

106392736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84482361-C-T

http://identifiers.org/hco/12/GRCh38#106392888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84482518-C-A

106392912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84482542-A-T

106393249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84482874-A-T

106393605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84483557-G-C

http://identifiers.org/hco/12/GRCh38#106393769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84483715-C-A

http://identifiers.org/hco/12/GRCh38#106393806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84483879-C-A

106393998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84484105-A-G

106394296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84484362-G-A

106394502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84484553-C-T

106394773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84484791-A-G

106396069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84485640-C-G

http://identifiers.org/hco/12/GRCh38#106405014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84487632-C-A

106405065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84487682-T-C

106405520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488223-C-G

106405724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488397-A-T

http://identifiers.org/hco/12/GRCh38#106405726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84488399-C-A

http://identifiers.org/hco/12/GRCh38#106405731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84488401-C-A

106405731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488401-C-G

106405731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488401-C-T

106406105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488765-G-A

106406105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488765-G-T

http://identifiers.org/hco/12/GRCh38#106406125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84488785-C-A

106406125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84488785-C-T

106406723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489015-T-G

106406725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489017-A-G

106406789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489058-C-T

106407146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489319-C-G

106407146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489319-C-T

http://identifiers.org/hco/12/GRCh38#106407234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84489407-A-C

106407318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489485-G-C

106407384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489550-A-G

106407840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84489684-A-T

106408627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84490101-G-A

106408627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84490101-G-C

106408729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84490191-A-G

106409163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84490547-G-C

106410567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84491565-G-A

106410583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84491581-A-G

106410583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84491581-A-T

http://identifiers.org/hco/12/GRCh38#106410604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84491601-C-A

106410623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491615-C-T

106410632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491623-T-C

106410636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491627-G-T

106410642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491633-A-G

106410656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491647-A-T

106410657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491648-T-C

106410734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491719-A-G

106410734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491719-A-T

106410742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491727-G-A

106410779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491762-T-C

106410815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84491798-C-G

http://identifiers.org/hco/12/GRCh38#106411087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84492069-C-A

106417776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84493184-A-G

106417801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84493209-C-T

106417881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84493285-A-G

106418518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84493907-C-T

106418641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84494031-C-T

106418696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84494086-T-C

106419058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84494442-G-A

106419718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495053-G-A

106419718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495053-G-T

106419841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495152-T-G

106420049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495341-C-T

106420079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495374-A-G

106420136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495422-A-G

106420197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495471-G-A

106420271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84495532-A-G

http://identifiers.org/hco/12/GRCh38#106420339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84495589-C-A

106420837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496068-C-G

106421023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496446-T-C

106421047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496467-G-A

106421047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496467-G-C

106421320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496655-G-T

106421489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496777-C-T

106421503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496791-T-C

http://identifiers.org/hco/12/GRCh38#106421526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84496814-C-A

106421526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496814-C-T

http://identifiers.org/hco/12/GRCh38#106421725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84496999-A-C

106421725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84496999-A-G

106424973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84501505-C-G

106425288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84501783-C-T

106425364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84501878-C-T

106425383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84501897-A-T

106425449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84501951-C-T

106425494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84501996-C-T

106425805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502283-T-G

106425913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502374-G-A

106426019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502474-T-C

106426064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502517-T-G

106426399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502605-C-T

106426525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502688-C-T

106426720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84502865-G-A

106427334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84503323-T-C

http://identifiers.org/hco/12/GRCh38#106427464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84503441-A-C

106427464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84503441-A-G

http://identifiers.org/hco/12/GRCh38#106427468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84503445-C-A

106427468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84503445-C-T

http://identifiers.org/hco/12/GRCh38#106428004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84504295-C-A

106428004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84504295-C-T

http://identifiers.org/hco/12/GRCh38#106428032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84504323-A-C

106428033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84504330-T-A

106428144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84504415-C-T

http://identifiers.org/hco/12/GRCh38#106428373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84507194-A-C

106428373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84507194-A-G

106428761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84507531-A-G

106429042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84507802-G-A

106429042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84507802-G-C

106429070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84507830-T-G

106429644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84508527-A-G

106430125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84509071-A-G

106430158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84509104-G-A

106430158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84509104-G-T

106430174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84509120-G-T

106430193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84509139-A-G

106430244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84509164-A-G

106430278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84509197-T-C

106430335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84509254-C-T

http://identifiers.org/hco/12/GRCh38#106430483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84509403-C-A

http://identifiers.org/hco/12/GRCh38#106432221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84510327-C-A

106432221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510327-C-T

http://identifiers.org/hco/12/GRCh38#106432267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84510372-C-A

106432267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510372-C-G

106432267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510372-C-T

http://identifiers.org/hco/12/GRCh38#106432280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84510383-A-C

106432280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510383-A-G

106432506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510609-G-A

106432506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510609-G-T

106432542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84510885-T-C

106432915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84512188-C-G

106433179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84512393-T-G

106433580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84512621-G-A

106433580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84512621-G-T

106433771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84512799-A-T

106434089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84513088-G-A

106434154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84513154-G-A

106435799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84514084-C-G

106435865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84514162-A-G

106436491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84514738-T-C

106436609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84514851-C-G

106436621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84514863-A-G

106436681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515261-A-G

106436802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515386-C-G

http://identifiers.org/hco/12/GRCh38#106436931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84515506-C-A

106436931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515506-C-G

106436988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515555-G-A

106437000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515568-G-T

106437005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515573-T-C

106437072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84515625-C-G

106437072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84515625-C-T

http://identifiers.org/hco/12/GRCh38#106437142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84515695-A-C

106437142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515695-A-T

106437163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84515716-C-T

106437449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516024-T-G

106437535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516091-C-T

106437560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516115-G-T

106437604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516158-C-T

106437613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516167-C-T

http://identifiers.org/hco/12/GRCh38#106437658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84516207-C-A

106437796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516342-G-A

http://identifiers.org/hco/12/GRCh38#106437818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84516370-C-A

106438737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84516607-A-T

106439746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84517099-T-C

106440436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84517490-T-A

106440480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84517528-A-G

106440556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84517581-G-A

106440740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84517717-T-C

106440972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84517896-G-A

http://identifiers.org/hco/12/GRCh38#106444327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84519915-C-A

106444327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84519915-C-T

106444550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84520128-G-A

106444651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520217-T-C

http://identifiers.org/hco/12/GRCh38#106444664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84520230-C-A

106444664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520230-C-T

106444701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520262-G-A

106444701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520262-G-T

106444983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520507-A-G

106445040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520578-C-T

106445267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520771-A-G

106445288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520793-C-T

106445451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520898-G-A

106445520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84520963-G-A

106445620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521042-A-G

106445621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521043-G-T

106445882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521245-A-G

106445896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521259-G-A

http://identifiers.org/hco/12/GRCh38#106445922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84521284-A-C

106446048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521409-A-G

106446240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521596-G-A

106446311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521662-C-G

106446311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521662-C-T

106446320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521672-G-A

http://identifiers.org/hco/12/GRCh38#106446418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84521765-A-C

http://identifiers.org/hco/12/GRCh38#106446419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84521766-A-C

106446424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521771-A-G

http://identifiers.org/hco/12/GRCh38#106446477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84521814-C-A

106446477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521814-C-T

106446530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521867-A-G

106446537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84521874-T-A

106446976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84522300-C-T

106447110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84522416-G-C

106447146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84522443-T-C

106451902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526184-C-G

106451951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526236-A-G

106451951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526236-A-T

106452074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526410-G-A

106452194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526518-A-T

106452386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526700-T-C

106452395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526709-A-G

106452445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526758-C-G

106452445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526758-C-T

106452497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526808-G-A

106452571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526882-G-A

106452571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84526882-G-C

106452914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84527229-A-G

106453479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84527508-A-G

http://identifiers.org/hco/12/GRCh38#106453533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84527560-A-C

http://identifiers.org/hco/12/GRCh38#106453845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84527833-C-A

106453859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84528020-T-A

106453897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84528059-C-T

106453977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84528149-A-G

http://identifiers.org/hco/12/GRCh38#106454181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84528294-A-C

106454274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84528404-A-T

http://identifiers.org/hco/12/GRCh38#106454364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84528530-A-C

106454365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84528531-T-C

106454677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84528836-T-C

106454677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: missense variant
orthologous variants: 84528836-T-G

106455793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84530355-C-G

http://identifiers.org/hco/12/GRCh38#106456784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84530671-A-C

106456998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84530831-C-G

106456998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84530831-C-T

106457346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531634-T-A

106457349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531637-T-C

http://identifiers.org/hco/12/GRCh38#106457408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84531695-C-A

106457408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531695-C-G

106457418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531705-A-G

106457570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531847-G-A

106457570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531847-G-T

106457685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84531963-A-G

106457901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84532178-G-A

106457901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84532178-G-T

http://identifiers.org/hco/12/GRCh38#106458930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84532630-C-A

http://identifiers.org/hco/12/GRCh38#106459219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84532781-C-A

106459219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84532781-C-T

106459339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: synonymous variant
orthologous variants: 84532901-G-A

106459394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84532945-T-C

106459498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533117-T-C

106459678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533248-G-T

106459726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533296-A-G

106459891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533435-T-C

106460001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533541-A-T

106460370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533744-G-C

106460373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84533747-C-T

106460656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84534010-G-T

106460868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84534207-G-A

http://identifiers.org/hco/12/GRCh38#106463361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84535158-C-A

106463361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535158-C-T

http://identifiers.org/hco/12/GRCh38#106463385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84535182-C-A

106463385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535182-C-T

106463414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535210-T-C

106463725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535424-A-G

106463725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535424-A-T

http://identifiers.org/hco/12/GRCh38#106463770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84535448-C-A

106463770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535448-C-T

106463800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535475-C-T

106463959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535601-A-G

106464013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535650-A-G

106465245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84535709-G-T

106478252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84536517-C-T

106478589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84536837-C-T

106478596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84536844-A-G

106486332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84539975-G-T

106486341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84539984-A-T

106486369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540007-G-T

106486519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540144-A-G

106486587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540163-G-A

106486588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540164-C-T

106486777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540330-T-C

106487311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540764-C-G

106487311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540764-C-T

106487330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84540783-G-C

http://identifiers.org/hco/12/GRCh38#106487337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84540790-A-C

106487591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84541044-G-C

106487822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84541283-A-G

106488035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84541519-G-A

106488160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84541676-A-G

106488171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84541691-A-G

106488760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84542246-T-C

106489606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84543051-G-C

106489772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84543223-G-A

106490032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84543447-C-T

106490033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84543448-G-A

106490081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84543511-T-C

106490638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84544070-G-A

106490981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84544377-A-G

106492084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84545335-A-G

106493205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84546365-G-A

106493215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84546375-T-A

106493250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84546409-T-C

106493411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84546584-A-G

106493478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84546648-T-A

106494096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84547296-T-G

http://identifiers.org/hco/12/GRCh38#106494166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84547362-A-C

106494314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84547473-C-T

106494358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84547520-C-T

106494836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84547963-A-G

106494899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84548027-T-G

http://identifiers.org/hco/12/GRCh38#106494906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84548034-A-C

106494965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84548185-G-T

106495378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84548615-A-G

106495526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84548749-A-G

106495880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84549320-G-A

106495880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84549320-G-C

106495880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84549320-G-T

106495937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron variant
orthologous variants: 84549377-A-G

106496119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84549557-C-G

106496119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84549557-C-T

106496183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84549621-A-G

http://identifiers.org/hco/12/GRCh38#106496485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84549849-C-A

106496487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84549851-C-T

http://identifiers.org/hco/12/GRCh38#106496512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84549876-A-C

106496823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84550180-G-A

106498900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84551688-G-A

http://identifiers.org/hco/12/GRCh38#106499181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84551984-A-C

106499181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84551984-A-G

106499396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84552263-A-G

106499397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84552264-G-T

106499541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84552389-A-G

106499888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84552685-C-T

http://identifiers.org/hco/12/GRCh38#106500076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84552861-C-A

106500076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 84552861-C-G

106500076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 84552861-C-T

106500081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84552866-G-A

106500081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84552866-G-T

http://identifiers.org/hco/12/GRCh38#106500136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84552910-C-A

106500136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84552910-C-T

106500296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553055-T-C

106500323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553078-A-G

106500422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553172-C-G

106500485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553221-G-A

106500485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553221-G-T

106500841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553730-A-G

http://identifiers.org/hco/12/GRCh38#106500895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84553826-A-C

106500895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553826-A-G

106500896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84553827-G-A

106501056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84554022-A-G

http://identifiers.org/hco/12/GRCh38#106501211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84554148-C-A

106501211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84554148-C-T

http://identifiers.org/hco/12/GRCh38#106501284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84554237-C-A

106501284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84554237-C-T

http://identifiers.org/hco/12/GRCh38#106501341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#84554292-C-A

106501362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84554313-C-T

106501387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84554338-C-T

106503946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84556091-G-A

106504006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84556145-C-T

106504102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84556229-T-C

106504105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84556232-T-C

106504216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84556343-T-C

106504222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84556349-T-C

http://identifiers.org/hco/12/GRCh38#106504363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84556487-C-A

106504363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84556487-C-G

106504434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84556560-A-G

106504513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84556638-C-T

106505036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557037-G-A

106505036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557037-G-T

106505383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557382-G-A

106505390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557389-C-T

106506035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557875-G-A

106506118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557960-G-T

106506126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84557968-C-T

106506163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558005-G-A

106506268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558101-A-T

106506272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558105-T-C

106506475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558283-C-T

106506538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558338-C-G

106506703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558467-T-C

106506839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558591-G-T

106506903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84558654-G-A

106507486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84559188-A-T

106507500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84559202-A-G

http://identifiers.org/hco/12/GRCh38#106507539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84559232-C-A

106507539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84559232-C-T

106508506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84560771-A-G

106509160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84561316-G-C

106509165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84561321-A-G

106509177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84561333-A-G

106509274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84561428-T-C

106509306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84561443-A-G

106509323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84561450-T-A

106509447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84561542-C-T

106509468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84561563-G-A

106509468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84561563-G-T

http://identifiers.org/hco/12/GRCh38#106509861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84562135-A-C

106509900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84562157-T-G

106510124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84562718-A-G

106510193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84562746-A-G

106510193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84562746-A-T