104781464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53031234-A-G

104781602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53031370-T-C

104781909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53031655-T-C

http://identifiers.org/hco/9/GRCh38#104782196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53031903-C-A

104782308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032005-C-G

104782606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032276-T-G

104782855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032522-A-T

104782951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032605-G-A

104782951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032605-G-T

104783035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032672-G-T

104783097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032722-T-C

104783353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53032984-C-T

http://identifiers.org/hco/9/GRCh38#104783569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53033208-C-A

104783740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53033375-G-C

104783859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53033493-C-T

104783860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53033494-G-A

104783860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53033494-G-T

http://identifiers.org/hco/9/GRCh38#104783937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53033572-C-A

104784117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53033745-G-A

http://identifiers.org/hco/9/GRCh38#104784365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53033993-C-A

104784468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53034094-T-G

104784477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53034103-C-T

104784571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53034205-T-C

104784571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53034205-T-G

104784586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53034220-G-A

104785145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035111-T-C

http://identifiers.org/hco/9/GRCh38#104785313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53035257-C-A

104785313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035257-C-G

http://identifiers.org/hco/9/GRCh38#104785316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53035260-C-A

104785316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035260-C-T

104785322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035266-G-A

104785322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035266-G-T

104785464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53035405-T-C

104785464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53035405-T-G

104785686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035633-T-C

104785694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035641-A-T

104785787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035722-A-G

104785822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035756-C-T

http://identifiers.org/hco/9/GRCh38#104785833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53035767-A-C

104785886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035816-T-C

104785922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035853-C-G

104785951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035888-G-T

104785952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035889-C-G

104786050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53035985-G-C

104786218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036149-G-A

104786218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036149-G-T

http://identifiers.org/hco/9/GRCh38#104786220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53036151-C-A

http://identifiers.org/hco/9/GRCh38#104786223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53036176-C-A

104786227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036180-T-C

http://identifiers.org/hco/9/GRCh38#104786235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53036188-C-A

104786258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036215-T-A

104786422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036386-A-G

104786423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036387-G-A

104786423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036387-G-C

104786425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036389-G-C

104786448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036413-C-T

104786515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036478-T-C

104786537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036501-A-G

104786540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036504-G-T

104786724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036702-T-G

104786733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036726-G-A

104786863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53036861-T-C

104787014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53037011-G-A

104787014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53037011-G-T

104787217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53037293-A-G

104787350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53037435-T-C

104787577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53037639-T-C

http://identifiers.org/hco/9/GRCh38#104787709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53037808-A-C

104787709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53037808-A-G

104787722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53037821-G-T

104787732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53037831-G-A

104787732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53037831-G-T

104787756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53037854-T-C

http://identifiers.org/hco/9/GRCh38#104787774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53037872-C-A

104787880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038102-C-T

104787938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53038175-C-T

104788058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 53038295-C-T

104788097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038335-A-T

http://identifiers.org/hco/9/GRCh38#104788105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53038343-A-C

104788147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038384-T-A

104788148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038385-A-G

104788177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038402-A-T

http://identifiers.org/hco/9/GRCh38#104788275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53038488-C-A

104788275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038488-C-G

104788275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038488-C-T

104788276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038492-C-T

104788312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038513-G-A

104788312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038513-G-T

104788325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038526-T-A

104788325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038526-T-G

http://identifiers.org/hco/9/GRCh38#104788338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53038537-C-A

104788338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038537-C-T

104788369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038571-G-T

104788410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038603-C-T

104788447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53038640-G-A

104788489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53038682-A-G

http://identifiers.org/hco/9/GRCh38#104788584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53038776-A-C

104788584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038776-A-G

104788586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038778-C-G

104788593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038785-G-C

104788593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038785-G-T

104788658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038852-C-G

104788658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038852-C-T

http://identifiers.org/hco/9/GRCh38#104788660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53038854-C-A

104788684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038872-T-C

104788704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038892-G-A

104788704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038892-G-T

104788754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038940-C-T

104788853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53038991-C-T

104789099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53039418-G-A

104789221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53039530-C-T

104789311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53039619-T-C

104789718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53040006-T-G

104790359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53040216-G-A

104790813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53040611-T-C

104790821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53040619-A-G

http://identifiers.org/hco/9/GRCh38#104790883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53040681-A-C

104790883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53040681-A-G

104790886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53040684-T-C

104790963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53040760-A-G

104791036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53040833-G-A

104791038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53040835-A-G

http://identifiers.org/hco/9/GRCh38#104791090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53040913-A-C

http://identifiers.org/hco/9/GRCh38#104791121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53040947-A-C

104791135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53040966-A-G

104791151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53041012-G-A

104791151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53041012-G-T

http://identifiers.org/hco/9/GRCh38#104791172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53041036-A-C

104791172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53041036-A-G

104791798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53041400-T-A

104791798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53041400-T-C

104791827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53041429-C-T

http://identifiers.org/hco/9/GRCh38#104792108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#53041712-C-A

104792134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53041732-T-A

104792346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53041876-T-C

104792581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042091-G-T

104792588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042097-T-G

104792590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042099-T-A

104792657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042174-G-T

104792687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042207-C-T

104792702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042232-T-G

104792778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53042303-T-A

104792778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53042303-T-C

http://identifiers.org/hco/9/GRCh38#104792828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53042356-A-C

104792839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53042367-T-C

104792867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53042395-A-G

http://identifiers.org/hco/9/GRCh38#104792993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53042524-C-A

104792996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042527-G-T

104793041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042560-C-T

104793047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042567-G-A

104793047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042567-G-T

http://identifiers.org/hco/9/GRCh38#104793062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53042582-C-A

http://identifiers.org/hco/9/GRCh38#104793077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53042587-C-A

104793077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042587-C-T

104793099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042609-G-T

104793115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042620-G-T

104793127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042632-T-C

104793127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042632-T-G

http://identifiers.org/hco/9/GRCh38#104793263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53042756-C-A

104793337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53042833-G-A

104793433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043153-G-A

104793433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043153-G-C

104793433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043153-G-T

http://identifiers.org/hco/9/GRCh38#104793610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53043320-C-A

104793610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043320-C-T

104793829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043524-T-G

104793909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043597-T-C

104794024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043713-G-C

104794026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043715-A-G

104794108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043840-G-A

104794140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043875-T-C

104794180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043922-A-G

104794184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043926-T-C

104794195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043937-C-G

104794225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53043967-C-T

104794325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044058-T-A

http://identifiers.org/hco/9/GRCh38#104794371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53044099-C-A

104794371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044099-C-T

104794433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53044161-G-A

http://identifiers.org/hco/9/GRCh38#104794457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53044185-A-C

104794502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53044230-A-T

104794507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53044235-G-A

104794507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53044235-G-C

104794507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53044235-G-T

104794546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044262-G-A

104794546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044262-G-C

104794546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044262-G-T

http://identifiers.org/hco/9/GRCh38#104794583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53044296-C-A

104794583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044296-C-T

104794621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044334-A-T

104794683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044385-C-T

104794861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044530-T-A

104794872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044541-A-G

104794971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044747-A-G

104794980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044756-G-A

104795005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044779-C-G

104795048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53044822-T-C

104795338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045132-C-G

104795401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045173-G-A

104795451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045213-T-C

104795668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045403-A-G

104795753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045475-G-A

104795754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045476-C-T

104795810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045544-T-A

104795810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045544-T-C

104795810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045544-T-G

104795954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045675-C-T

http://identifiers.org/hco/9/GRCh38#104795966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53045687-C-A

104795966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045687-C-G

104795966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045687-C-T

104795991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045712-C-G

104795997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045718-C-T

104796003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045724-G-C

104796003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045724-G-T

104796006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045727-C-G

104796006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045727-C-T

104796024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045761-A-G

http://identifiers.org/hco/9/GRCh38#104796065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53045787-C-A

104796173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53045895-G-A

104796216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045936-A-G

104796279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045999-G-A

104796279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53045999-G-C

104796431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53046152-G-A

http://identifiers.org/hco/9/GRCh38#104796477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53046191-C-A

104796503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53046215-G-A

104796503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53046215-G-T

104796769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53046481-G-A

104796856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53046568-A-T

104797018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53046744-A-G

104797250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53046977-G-A

104797773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53047440-G-A

104798115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53047809-G-C

104798271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53048804-G-T

104798274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53048807-A-G

http://identifiers.org/hco/9/GRCh38#104798279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53048812-C-A

104798279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53048812-C-T

104798333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53048866-G-A

104798333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53048866-G-T

104798335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53048868-T-C

104798457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53048992-A-G

104798691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53049199-T-C

104798871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53049382-G-A

104798884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53049398-C-T

104799126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53049660-C-T

104799136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53049670-T-G

104799423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53049936-C-T

http://identifiers.org/hco/9/GRCh38#104799605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53050092-C-A

104799693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050176-T-C

104799774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050252-C-G

104799779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050259-C-T

104799830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53050300-T-G

http://identifiers.org/hco/9/GRCh38#104800230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53050656-C-A

104800372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050806-G-A

104800372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050806-G-T

104800405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050839-C-G

104800427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53050861-C-G

104800679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051087-G-A

104800679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051087-G-T

104800712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051123-T-A

104800712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051123-T-C

104800909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051483-C-T

104800988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051651-T-C

104801092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051742-G-A

http://identifiers.org/hco/9/GRCh38#104801114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53051764-C-A

104801114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051764-C-T

http://identifiers.org/hco/9/GRCh38#104801200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53051858-C-A

104801200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53051858-C-T

104802031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059234-A-G

104802034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059237-T-A

104802129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53059332-A-G

104802178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059381-A-G

http://identifiers.org/hco/9/GRCh38#104802191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53059394-C-A

104802191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059394-C-G

104802226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059422-G-A

104802226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059422-G-T

104802228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059424-G-A

104802228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059424-G-T

104802235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059428-T-C

104802237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059430-T-A

104802249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059442-T-A

104802249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059442-T-C

104802492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059609-G-C

104802523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059623-C-T

104802528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53059628-G-A

104802984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060044-C-G

104803261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060296-G-A

104803330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060382-G-A

104803377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060422-T-A

104803378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060423-G-A

104803378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060423-G-T

104803409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060458-A-G

http://identifiers.org/hco/9/GRCh38#104803415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53060464-C-A

104803415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060464-C-T

104803501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53060541-C-T

104804140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061066-A-G

104804193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061119-G-A

104804480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061386-A-T

104804492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061397-T-C

104804546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061441-G-A

104804546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061441-G-T

104804547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061442-T-G

104804561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061455-T-C

104804561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061455-T-G

104804621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061482-G-T

104804748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061609-G-A

104804748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061609-G-C

104804748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061609-G-T

http://identifiers.org/hco/9/GRCh38#104804848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53061677-C-A

104804848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061677-C-T

104804861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061690-A-G

104804921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53061736-G-T

104806349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53062498-C-G

104806385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53062534-T-C

104806385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53062534-T-G

104806683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53062803-C-T

104806822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53062935-G-T

104807010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063279-G-A

104807055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063323-A-G

104807055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063323-A-T

104807105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063361-G-A

104807227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063478-C-G

104807269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063518-C-T

http://identifiers.org/hco/9/GRCh38#104808008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53063827-C-A

104808058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063876-A-G

104808179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53063992-C-T

104808303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53064113-C-T

104808309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53064119-C-G

104808881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53065379-C-T

104809094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53065562-G-A

104809363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53065810-G-A

104809363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53065810-G-T

104809420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53065855-A-G

http://identifiers.org/hco/9/GRCh38#104809423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53065858-C-A

104809423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53065858-C-T

104809498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53065933-G-A

104809498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53065933-G-T

104809537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53065972-G-T

104809568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53066003-T-C

104809597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066032-A-G

104809598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066033-T-C

104809672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066106-A-G

104809850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066266-T-C

104810067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066465-G-A

104810181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066581-T-A

104810186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066586-G-T

104810210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066606-A-G

104810306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066700-T-C

104810464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066780-C-T

http://identifiers.org/hco/9/GRCh38#104810656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53066882-C-A

104810706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066932-C-T

104810714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066940-T-C

104810753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066985-G-A

104810753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53066985-G-T

104810946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53067177-G-A

104810959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53067188-C-T

104811011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53067232-C-G

104811068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53067292-G-T

104811682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53067944-G-A

104812288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53068500-C-T

http://identifiers.org/hco/9/GRCh38#104812471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53068614-C-A

104812471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53068614-C-T

104812511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53068654-T-G

104812607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53068720-A-G

104812667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53068780-C-T

http://identifiers.org/hco/9/GRCh38#104812688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53068801-A-C

104812688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53068801-A-G

104812709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53068822-T-C

104812774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53068890-T-C

104812993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53069077-G-A

104813075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53069121-G-A

104814009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53069686-T-C

104814083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53069761-A-G

104814148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53069822-C-T

http://identifiers.org/hco/9/GRCh38#104814253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53069927-C-A

104814257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53069931-T-C

104814366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070020-C-T

104814508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070159-C-G

http://identifiers.org/hco/9/GRCh38#104814510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53070161-C-A

104814510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070161-C-T

104814552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070200-T-G

104814565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070213-G-A

104814565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070213-G-T

http://identifiers.org/hco/9/GRCh38#104814598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53070245-C-A

104814598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070245-C-T

104814668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070311-T-C

104815345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070656-T-A

104815345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070656-T-C

http://identifiers.org/hco/9/GRCh38#104815423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53070728-A-C

104815428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070733-C-T

104815481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53070785-G-A

104816102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53071814-T-C

104816170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53071850-A-G

104816218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53071898-G-T

104816371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072050-G-A

104816403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072078-G-A

104816456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072133-T-A

104816456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072133-T-C

104816457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072134-G-T

http://identifiers.org/hco/9/GRCh38#104816460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53072137-C-A

104816460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072137-C-T

104816473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072150-T-A

104816473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072150-T-C

http://identifiers.org/hco/9/GRCh38#104816481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53072158-C-A

104816496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072173-T-C

104816984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072537-C-T

104817076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072637-G-T

http://identifiers.org/hco/9/GRCh38#104817088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53072650-C-A

104817104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072666-C-G

104817105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53072667-T-C

104817509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073077-T-A

104817509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073077-T-G

http://identifiers.org/hco/9/GRCh38#104817539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53073108-C-A

104817539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073108-C-T

104817569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073137-T-C

104817585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073155-C-G

104817585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073155-C-T

104817634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073204-G-C

104817821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073388-C-T

104818035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073611-A-G

104818285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073839-G-T

104818345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53073898-A-G

104818546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074102-G-T

104818575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074132-A-T

http://identifiers.org/hco/9/GRCh38#104818586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53074144-A-C

104818586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074144-A-T

104818912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074477-A-G

104818923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074487-C-T

http://identifiers.org/hco/9/GRCh38#104818932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53074496-C-A

104818950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074514-A-G

http://identifiers.org/hco/9/GRCh38#104818992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53074556-C-A

104818992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074556-C-T

http://identifiers.org/hco/9/GRCh38#104819026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53074578-C-A

104819026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074578-C-T

104819395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074974-G-C

104819395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53074974-G-T

104819433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075011-G-C

http://identifiers.org/hco/9/GRCh38#104819437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53075015-C-A

104819437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075015-C-T

104819442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075020-T-C

104819531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075080-A-G

104819604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53075149-G-A

http://identifiers.org/hco/9/GRCh38#104819686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53075231-A-C

104819763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075294-C-T

http://identifiers.org/hco/9/GRCh38#104819791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53075348-A-C

104819827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075381-G-A

104819827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075381-G-T

104819918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075438-G-A

104819918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075438-G-T

104819921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075441-C-T

104820009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53075529-G-A

104820036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53075556-G-A

104820108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075629-G-T

104820110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075631-T-C

104820131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075641-C-T

104820197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075693-A-G

http://identifiers.org/hco/9/GRCh38#104820243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53075713-C-A

104820307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075768-G-A

104820321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075782-C-G

104820324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075785-G-A

104820478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53075909-C-T

http://identifiers.org/hco/9/GRCh38#104820707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53076129-C-A

104820707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53076129-C-T

104820758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53076166-G-A

104821261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53076728-A-G

104821299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53076776-G-C

104821343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53076819-A-G

104821524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077039-G-A

104821557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077071-C-T

http://identifiers.org/hco/9/GRCh38#104821568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53077082-C-A

104821610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077122-G-A

104821610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077122-G-C

104821610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077122-G-T

http://identifiers.org/hco/9/GRCh38#104821648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53077175-C-A

104821648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077175-C-T

104821690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077214-G-T

104821960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077449-A-T

http://identifiers.org/hco/9/GRCh38#104822055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53077532-C-A

104822179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077619-T-C

104822245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077722-T-C

104822348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077817-G-T

104822352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077821-A-T

104822375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077829-A-G

104822383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077838-T-G

104822405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53077859-G-T

104822760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078214-T-C

104822815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078265-T-C

104823043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078483-T-A

104823043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078483-T-C

104823043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078483-T-G

104823063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078504-T-A

104823063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53078504-T-G

104824034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079170-T-A

104824034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079170-T-C

104824208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079350-G-A

104824225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079367-A-G

104824320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079435-T-C

104824596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079711-G-A

104824596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079711-G-C

104824680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079794-G-C

104824712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079813-G-C

104824712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53079813-G-T

http://identifiers.org/hco/9/GRCh38#104824731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53079832-C-A

http://identifiers.org/hco/9/GRCh38#104824958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53080063-C-A

104824990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080091-A-G

104825086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080177-A-G

104825274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080356-G-A

104825324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080404-T-C

104825345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080426-G-C

104825353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080434-C-T

104825355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080436-T-A

104825460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080525-T-C

104825483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080548-G-A

104825483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53080548-G-T

104825596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53080660-A-G

104825646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53080717-A-T

104825702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53080785-G-A

104825806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53080889-C-T

http://identifiers.org/hco/9/GRCh38#104825934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53081018-A-C

104825975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081055-T-C

104825975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081055-T-G

104826012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081092-G-T

104826264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081332-G-A

104826283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081349-T-A

104826298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081364-G-A

104826362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081425-T-C

104826879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081866-C-T

104826884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53081871-A-T

104827217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082191-C-T

104827250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082218-G-C

104827250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082218-G-T

104827273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082241-G-T

104827285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082253-G-T

104827292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082260-G-T

http://identifiers.org/hco/9/GRCh38#104827293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53082261-C-A

104827293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082261-C-T

http://identifiers.org/hco/9/GRCh38#104827314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53082282-C-A

104827516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082474-G-C

104827768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082742-A-G

http://identifiers.org/hco/9/GRCh38#104827899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53082881-A-C

104827996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53082982-G-A

104828168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083159-C-T

104828252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083247-A-G

104828252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083247-A-T

104828433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083351-A-G

104828433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083351-A-T

104828488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083396-C-T

104828865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083667-T-G

104829075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53083876-C-T

104829093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53083894-C-G

104829171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083972-G-A

104829171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083972-G-C

104829171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53083972-G-T

104829228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084017-G-C

104829228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084017-G-T

104829229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084018-G-A

http://identifiers.org/hco/9/GRCh38#104829247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084036-A-C

104829335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084112-C-G

104829382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084159-A-G

http://identifiers.org/hco/9/GRCh38#104830869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084328-A-C

104830963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53084422-A-G

104831108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53084567-C-T

http://identifiers.org/hco/9/GRCh38#104831164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084613-A-C

104831169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084618-A-T

http://identifiers.org/hco/9/GRCh38#104831178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084627-A-C

104831178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084627-A-G

http://identifiers.org/hco/9/GRCh38#104831179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084628-A-C

http://identifiers.org/hco/9/GRCh38#104831196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084645-C-A

104831196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084645-C-T

104831218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084667-T-A

104831218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084667-T-C

104831218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084667-T-G

104831441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084953-T-C

http://identifiers.org/hco/9/GRCh38#104831476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53084983-C-A

104831487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53084994-A-G

104831584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085071-T-C

104831584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085071-T-G

104831607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085081-T-C

104831804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53085278-T-C

104831885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085361-G-A

104831885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085361-G-T

104831902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085378-A-G

104831922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085399-A-G

http://identifiers.org/hco/9/GRCh38#104831934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53085411-C-A

104831934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085411-C-G

104831934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085411-C-T

http://identifiers.org/hco/9/GRCh38#104831939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53085416-C-A

104832251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085697-T-C

104832380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085816-T-C

104832382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085818-T-A

104832509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085926-T-C

104832509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085926-T-G

104832511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53085928-T-C

104832675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53086094-G-A

104832715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53086134-T-C

104832715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53086134-T-G

104832816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53086236-T-A

104833486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53086458-C-G

104833732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53086662-C-T

104833990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53086889-A-G

104834233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53087126-C-T

104834278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53087171-T-C

104835490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53087369-G-A

104835742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53087589-G-A

104836171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53088970-G-A

104836174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53088973-T-C

104836628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089430-A-T

104836632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089434-A-T

104836730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089569-C-G

104836871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089698-G-A

104836871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089698-G-C

104836871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089698-G-T

104836961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089780-T-A

104836965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089784-G-A

104836965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089784-G-T

104837112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089931-G-A

104837112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089931-G-C

104837112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53089931-G-T

104837206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090025-T-A

104837206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090025-T-G

104837231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090050-G-A

104837231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090050-G-T

104837240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090058-T-C

104837298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090123-G-A

104837298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090123-G-T

104837321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090148-A-G

104837349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090177-C-T

104837402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090229-G-C

104837464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53090290-T-G

104837690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090527-A-G

104837692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090529-A-G

104837693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090530-A-G

http://identifiers.org/hco/9/GRCh38#104837718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53090559-C-A

104837761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090611-G-A

104837769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53090619-G-A

http://identifiers.org/hco/9/GRCh38#104837894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53090722-A-C

104839066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091343-T-C

104839102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091379-C-T

http://identifiers.org/hco/9/GRCh38#104839159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53091438-C-A

104839159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091438-C-G

104839171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091450-G-A

104839171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091450-G-C

104839192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091475-T-C

104839376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091650-G-A

104839377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53091651-T-C

104840094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53092488-A-G

104840130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53092520-T-A

104840130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53092520-T-C

104840306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53092756-C-T

104840385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53092835-C-T

104840457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53092907-G-A

104840532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53092981-A-G

104840570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093011-G-T

http://identifiers.org/hco/9/GRCh38#104842567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53093251-C-A

104842576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093260-A-G

104842652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093335-A-G

104842689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093359-T-C

104842748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093416-A-T

http://identifiers.org/hco/9/GRCh38#104842752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53093419-C-A

104842991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093556-G-A

104842991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093556-G-T

http://identifiers.org/hco/9/GRCh38#104843275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53093822-C-A

104843658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53093945-A-G

http://identifiers.org/hco/9/GRCh38#104844006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53094268-C-A

104844006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094268-C-T

104844052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094307-T-A

104844052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094307-T-G

104844207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094459-T-A

104844232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094482-C-T

http://identifiers.org/hco/9/GRCh38#104844266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53094500-C-A

104844387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094617-A-G

104844435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53094665-A-T

104844923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53095035-T-C

104844964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53095075-C-G

104845097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53095206-G-T

104845276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53095386-C-G

http://identifiers.org/hco/9/GRCh38#104845407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53095516-C-A

104845407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53095516-C-T

104845470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53095578-A-G

104845513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53095621-T-A

http://identifiers.org/hco/9/GRCh38#104845538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53095646-C-A

http://identifiers.org/hco/9/GRCh38#104845700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53095803-A-C

104845700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53095803-A-G

104845911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53096085-G-A

104845911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53096085-G-C

104845912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53096086-G-T

104846116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53096312-T-C

http://identifiers.org/hco/9/GRCh38#104846215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53096399-C-A

104846754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098139-C-G

104847000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098389-G-C

104847163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098530-G-A

104847230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098589-A-T

104847339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098645-T-C

104847343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098649-G-A

104847356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53098656-T-C

http://identifiers.org/hco/9/GRCh38#104849331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53099136-C-A

104849536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53099470-T-G

104849616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53099516-C-T

104849673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53099577-G-A

104849684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53099588-T-C

104849918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53100175-C-T

104850040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53100294-G-A

104850705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53100689-A-G

104850798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53100792-T-C

104851073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53101050-C-T

104851518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53101621-T-C

104851553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53101651-T-C

104852349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53102393-A-G

104852411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53102444-C-T

104852554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53102590-A-G

104852931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53103387-G-A

104853160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53103599-A-G

104855515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53104269-A-G

104855570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53104324-T-C

104855582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53104336-T-C

104855651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53104409-A-G

104855669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53104427-T-C

104855733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant
orthologous variants: 53104494-C-T

104855756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53104517-A-G

104855773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53104534-G-A

http://identifiers.org/hco/9/GRCh38#104855911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53104690-A-C

104855996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant
orthologous variants: 53104774-C-G

104856005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, missense_variant
orthologous variants: 53104783-C-G

104856005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 53104783-C-T

http://identifiers.org/hco/9/GRCh38#104856093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53104897-C-A

104856093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 53104897-C-T

104856195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53104997-A-G

http://identifiers.org/hco/9/GRCh38#104856216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53105012-A-C

104856230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105026-T-C

104856268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105063-C-T

104856274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105069-A-G

104856285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105080-C-T

104856368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105169-G-T

http://identifiers.org/hco/9/GRCh38#104856372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53105173-C-A

104856372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105173-C-T

http://identifiers.org/hco/9/GRCh38#104856412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53105210-C-A

104856452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105237-G-T

104856475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105250-G-A

104856494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105269-G-A

104856494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105269-G-T

104856536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53105302-T-A

104858085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53106602-G-A

104858159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53106670-C-T

http://identifiers.org/hco/9/GRCh38#104858210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53106728-A-C

http://identifiers.org/hco/9/GRCh38#104858422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53106934-C-A

104858422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53106934-C-T

104858469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53106981-A-G

104858615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: missense variant
orthologous variants: 53107099-T-G

104858929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53107384-A-G

104859067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53107519-T-C

104859421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53107894-A-G

104859444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53107918-G-A

104860284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53108258-G-A

http://identifiers.org/hco/9/GRCh38#104860312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53108286-A-C

104860694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53108661-T-C

104860694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53108661-T-G

104861137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109678-A-G

http://identifiers.org/hco/9/GRCh38#104861385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53108868-C-A

104861385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53108868-C-T

http://identifiers.org/hco/9/GRCh38#104861498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53108980-C-A

104861498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53108980-C-T

104861532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53109015-G-T

104861565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53109047-A-G

104861565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53109047-A-T

104861599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 53109083-G-A

104861703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53109188-C-T

104861876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109360-T-C

104861878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109362-G-A

104861878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109362-G-T

104862593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109764-G-A

104862593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109764-G-T

104862926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53109995-T-C

104863057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110166-T-C

104863235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110350-G-A

104863412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53110537-A-G

104863472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110593-C-G

104863476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110597-A-T

104863513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110628-G-T

http://identifiers.org/hco/9/GRCh38#104863772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53110842-C-A

104863777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110850-A-G

104863777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53110850-A-T

104864106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111173-T-C

http://identifiers.org/hco/9/GRCh38#104864112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53111183-C-A

104864112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111183-C-G

104864148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111220-G-C

104864374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111411-G-C

104864393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111436-G-A

104864436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111482-G-T

104864467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111577-G-T

104864552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111748-T-C

104864783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53111973-T-C

104865002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112183-G-A

http://identifiers.org/hco/9/GRCh38#104865098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53112286-A-C

http://identifiers.org/hco/9/GRCh38#104865201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53112386-A-C

104865244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112431-G-T

104865393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112510-G-A

104865510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112590-T-A

104865510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112590-T-C

104865510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112590-T-G

104865519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53112599-A-G

104866300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113001-C-T

104866305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113003-C-T

104866353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113045-G-T

104867189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113515-G-A

104867349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113907-C-T

104867400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113953-T-G

104867449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53113986-A-T

104867580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53114122-G-A

http://identifiers.org/hco/9/GRCh38#104868025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53114803-A-C

104868600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53115536-G-T

104868640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53115573-T-C

104868914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53115844-G-A

104868933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53115866-C-T

http://identifiers.org/hco/9/GRCh38#104868999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53115915-A-C

104869054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53115939-G-C

104869088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53115973-C-T

104869140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53116016-C-T

104869690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53116640-T-C

http://identifiers.org/hco/9/GRCh38#104869920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53116839-A-C

104870334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53117179-A-G

104871461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53117789-G-A

104871577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53117891-G-T

104871686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53118021-G-A

104871699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53118032-G-A

104871846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53118182-G-A

104871992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53118581-C-T

104872274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53118862-T-C

104872406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53118978-T-C

104872466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53119042-C-G

104872469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53119045-G-A

104872575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53119136-G-A

104872575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53119136-G-T

104872789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53119997-A-G

104873096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120281-G-A

104873106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120292-G-A

104873246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120425-T-C

104873413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120600-G-T

104873442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120651-G-A

104873442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120651-G-T

104873498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120695-C-G

104873629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53120806-C-T

104873901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121076-A-G

104873909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121083-A-T

104873927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121101-T-C

104875440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121378-A-G

104875814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121709-C-G

http://identifiers.org/hco/9/GRCh38#104875832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53121727-C-A

104875832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121727-C-T

104875938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121817-G-C

104875943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121822-T-C

104875992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121871-G-A

104875992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53121871-G-C

104876127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122012-C-T

104876329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122208-G-A

104876329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122208-G-C

104876365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122263-C-T

http://identifiers.org/hco/9/GRCh38#104876505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53122344-A-C

104876505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122344-A-G

104876545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122384-G-A

104876563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122401-G-T

104876760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122562-T-A

104876771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122573-G-A

104876771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122573-G-C

104876771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122573-G-T

104876928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122699-G-C

104876947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53122718-A-T

104877296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53123040-G-A

104877817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53123543-C-G

http://identifiers.org/hco/9/GRCh38#104878020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53123723-A-C

http://identifiers.org/hco/9/GRCh38#104878087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53123742-C-A

104878201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53123855-G-A

104878402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53124050-T-G

104878588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53124170-C-G

104879309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53125744-T-A

104881549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53126201-A-G

104881715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53126350-G-C

104882149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53126771-A-G

http://identifiers.org/hco/9/GRCh38#104882450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53127044-A-C

104882720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53127321-T-C

http://identifiers.org/hco/9/GRCh38#104882840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53127418-A-C

104883186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53127746-G-T

104883601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128044-T-A

104883601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128044-T-C

104883830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128212-A-G

104883842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128224-G-C

104883842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128224-G-T

104883881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128258-A-G

104884234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128566-C-T

http://identifiers.org/hco/9/GRCh38#104884355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53128655-C-A

104884412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128706-T-A

104884412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128706-T-C

104884456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53128750-G-A

104884456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53128750-G-C

104884492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53128786-G-A

104884543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53128837-G-A

104884543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: synonymous variant
orthologous variants: 53128837-G-C

104884558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 53128852-T-C

http://identifiers.org/hco/9/GRCh38#104884692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53128964-C-A

104884692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128964-C-T

104884694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128966-T-C

104884694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128966-T-G

104884696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53128968-T-C

104885258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53129420-A-G

104885574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53129727-A-G

104885667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53129812-A-G

http://identifiers.org/hco/9/GRCh38#104885670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53129815-C-A

104885670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53129815-C-T

104885823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53129947-C-T

104885972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53130090-T-C

104886045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53130164-G-A

104886206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53130900-C-T

http://identifiers.org/hco/9/GRCh38#104886819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53131488-C-A

http://identifiers.org/hco/9/GRCh38#104886866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53131537-A-C

104888210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53131785-T-A

104888565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132060-T-C

104888592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132086-T-C

104888968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132790-T-A

104888968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132790-T-C

104888968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132790-T-G

104889014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132836-T-C

104889025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53132847-G-T

http://identifiers.org/hco/9/GRCh38#104889136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53132956-A-C

104889136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 53132956-A-G

104889208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53133028-T-C

104889220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53133040-C-T

104889221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53133041-T-C

104889388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53133205-T-C

104889466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53133246-T-C

104889477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53133253-T-C

104892397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53134009-A-G

104892429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53134044-G-A

104892429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53134044-G-T

104893541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53134809-T-A

104893908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135181-C-T

104893950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135222-T-A

http://identifiers.org/hco/9/GRCh38#104894050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53135308-C-A

104894050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135308-C-T

104894143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135379-T-C

104894295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135487-G-A

104894305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135497-T-C

104894566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135758-G-A

104894599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53135786-C-T

104894977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53136158-C-T

104895185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53136358-G-A

104895274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53136443-C-T

104895366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53136537-T-C

104895366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53136537-T-G

http://identifiers.org/hco/9/GRCh38#104895713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53136814-C-A

104895857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53136954-A-G

http://identifiers.org/hco/9/GRCh38#104896103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53137295-C-A

104896103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53137295-C-T

104897222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138119-C-G

104897937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138548-A-G

104898038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138627-T-A

104898040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138629-A-G

104898099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138682-A-G

104898123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138700-G-A

104898134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138711-T-C

104898697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53138921-G-A

http://identifiers.org/hco/9/GRCh38#104898978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53139137-C-A

104899080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53139228-C-G

104899200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53139331-G-A

104899349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53139473-G-A

104899376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53139490-C-T

104899856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53139651-G-T

104900350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140061-C-G

104900350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140061-C-T

104900375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140085-C-T

104900554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140240-A-G

104900649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140309-G-A

104900649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140309-G-C

104900760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140417-G-A

104900813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140475-C-T

104901086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140760-A-G

104901127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140816-C-T

104901132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53140821-G-A

http://identifiers.org/hco/9/GRCh38#104901965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53142177-A-C

104902069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53142279-T-C

http://identifiers.org/hco/9/GRCh38#104902103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53142438-A-C

104902270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53142603-C-T

104902761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53143087-G-T

104903163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53143483-C-T

104903325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53143640-G-C

104903371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53143691-C-T

104903546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53143865-C-T

http://identifiers.org/hco/9/GRCh38#104903561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53143880-A-C

http://identifiers.org/hco/9/GRCh38#104903566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53143886-C-A

104903602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53143917-A-G

104903686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53144002-T-C

104903747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 53144071-C-T

http://identifiers.org/hco/9/GRCh38#104903785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53144109-C-A

104903785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53144109-C-T

104903919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53144271-A-G

104904165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53144505-T-C

104904592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53144613-T-A

104904592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53144613-T-C

104904640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53144661-T-C

104904988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145020-T-C

104905043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145073-G-A

104905071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145107-C-T

104905466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145480-T-A

104905487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145498-T-C

http://identifiers.org/hco/9/GRCh38#104905594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53145596-C-A

104905634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145668-G-A

104905891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145900-C-G

104905891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53145900-C-T

104906354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53146302-T-C

104906615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53146576-C-T

104906755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53146702-A-T

104907374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53147308-G-A

104907399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53147325-G-A

104907399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53147325-G-T

http://identifiers.org/hco/9/GRCh38#104907777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53147718-C-A

http://identifiers.org/hco/9/GRCh38#104908093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53148023-C-A

104908093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148023-C-T

104908760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148419-T-C

104908803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148465-G-C

104908816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148475-T-A

104908888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148547-G-A

104908905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148564-G-A

104909059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148751-A-G

104909245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53148943-G-A

104909465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149088-G-C

104909478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149101-G-A

104909547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149154-C-T

104909639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149230-C-T

104909655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149246-T-A

104909655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149246-T-C

104909818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149401-G-C

104909938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53149667-A-G

http://identifiers.org/hco/9/GRCh38#104910143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53149882-C-A

104910617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53150377-A-G

104910988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53150452-T-G

104911091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53150530-C-T

104911144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53150576-G-A

104911254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53150675-A-G

104911540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53150946-G-C

104911839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151184-C-T

104911942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151267-T-C

104911944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151269-T-C

104911982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151306-C-T

104911995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151323-T-G

104912139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151474-T-C

104912185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151538-T-A

104912494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151686-A-G

104912547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151748-C-T

104912589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151790-C-T

104912677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151880-G-A

104912787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53151992-A-G

104912940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152127-T-C

104912983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152170-T-G

104913341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152303-C-G

104913341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152303-C-T

104913369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152331-C-G

104913369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152331-C-T

104913493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152458-T-A

104913493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152458-T-C

104913715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53152682-T-G

104914991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153013-C-G

104915176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153178-G-A

104915176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153178-G-T

104915190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153192-C-T

104915296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153313-G-A

http://identifiers.org/hco/9/GRCh38#104915373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53153381-C-A

104915842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153833-G-C

http://identifiers.org/hco/9/GRCh38#104916025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53153929-C-A

104916028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53153932-G-A

http://identifiers.org/hco/9/GRCh38#104916160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53154068-C-A

104916160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154068-C-G

104916516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154415-C-T

104916532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154429-T-G

104916652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154545-C-T

http://identifiers.org/hco/9/GRCh38#104916898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53154807-A-C

104916912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154821-G-A

104916956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154868-G-C

104916958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154870-A-G

104916986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53154903-A-T

104921289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155293-C-G

104921289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155293-C-T

http://identifiers.org/hco/9/GRCh38#104921470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53155461-C-A

http://identifiers.org/hco/9/GRCh38#104921493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53155479-A-C

104921630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155594-T-C

104921891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155776-T-C

104921904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155786-G-A

http://identifiers.org/hco/9/GRCh38#104921985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53155844-A-C

104923445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53156439-G-A

104923518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53156513-T-G

104924112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53156772-G-A

104924869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53157223-C-G

104924869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53157223-C-T

104925065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53157403-G-A

104925408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53157443-T-C

104925517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53157560-A-G

104926056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53158066-T-C

104926396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53158537-C-T

104926436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53158577-G-A

104926436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: 53158577-G-C

http://identifiers.org/hco/9/GRCh38#104926445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53158586-C-A

104926509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53158655-A-G

104926591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53158739-C-T

104926626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, undefined
orthologous variants: 53158774-G-A

104927365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159162-C-G

104927438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159231-T-A

104927438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159231-T-C

104927482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159272-G-A

104927598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159351-A-G

104927598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159351-A-T

http://identifiers.org/hco/9/GRCh38#104927600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53159353-C-A

104927600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159353-C-T

104927675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159422-G-T

http://identifiers.org/hco/9/GRCh38#104927688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53159435-C-A

104927765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159512-T-C

104927874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53159625-A-G

104927999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53159741-G-A

http://identifiers.org/hco/9/GRCh38#104928030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#53159768-C-A

104928030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53159768-C-G

104928030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53159768-C-T