http://identifiers.org/hco/6/GRCh38#122996254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500578-A-C

122996254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500578-A-G

http://identifiers.org/hco/6/GRCh38#122996274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500555-C-A

122996274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500555-C-G

122996274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500555-C-T

http://identifiers.org/hco/6/GRCh38#122996299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500547-C-A

122996299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500547-C-T

122996342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500508-C-T

http://identifiers.org/hco/6/GRCh38#122996354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500494-C-A

122996354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500494-C-T

122996355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500493-C-T

122996360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500488-T-A

122996360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500488-T-C

122996369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500478-G-A

122996369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500478-G-T

122996373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500474-C-T

122996407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500445-G-T

122996408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500444-G-A

http://identifiers.org/hco/6/GRCh38#122996428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500423-C-A

122996428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500423-C-T

http://identifiers.org/hco/6/GRCh38#122996440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500415-C-A

122996440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500415-C-T

http://identifiers.org/hco/6/GRCh38#122996615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500260-C-A

122996659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500220-T-C

http://identifiers.org/hco/6/GRCh38#122996668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500211-C-A

122996668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500211-C-T

122996672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500207-G-A

122996672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500207-G-T

http://identifiers.org/hco/6/GRCh38#122996676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33500203-C-A

122996676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5 prime UTR variant
orthologous variants: 33500203-C-T

122996889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33499984-C-T

122996924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33499951-G-C

122996938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33499937-A-T

122997119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33499762-A-T

122997237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499657-G-A

122997264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499626-T-C

122997264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499626-T-G

122997311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499579-G-A

122997311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499579-G-T

122997422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499481-G-A

122997422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499481-G-T

122997449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499225-T-A

122997526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499175-G-C

122997566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499143-A-T

http://identifiers.org/hco/6/GRCh38#122997567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33499142-A-C

122997567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499142-A-G

122997567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499142-A-T

http://identifiers.org/hco/6/GRCh38#122997577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33499132-C-A

122997577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499132-C-T

122997598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499116-T-A

122997598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499116-T-C

122997598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499116-T-G

http://identifiers.org/hco/6/GRCh38#122997605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33499109-A-C

122997605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33499109-A-T

122997719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33498985-G-A

122997796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, missense_variant
orthologous variants: 33498908-G-A

122997796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, missense_variant
orthologous variants: 33498908-G-T

122997997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, stop_gained
orthologous variants: 33498707-C-T

http://identifiers.org/hco/6/GRCh38#122998038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33498666-A-C

122998199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498463-T-G

122998203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498459-T-G

122998236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498426-T-C

122998253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498409-T-C

122998253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498409-T-G

122998255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498407-A-G

122998292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498371-A-G

122998315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498335-G-T

122998414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498243-G-A

122998414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498243-G-C

122998493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498162-G-A

122998493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498162-G-C

122998581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498075-A-G

122998613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33498038-G-A

122998786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33497868-A-G

122998957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33497703-C-G

122999078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33497583-T-A

http://identifiers.org/hco/6/GRCh38#122999380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33497316-C-A

122999725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33497026-G-C

122999728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33497023-C-T

122999800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496940-G-A

http://identifiers.org/hco/6/GRCh38#122999838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33496893-C-A

122999857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496857-A-G

122999929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496781-T-A

122999929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496781-T-C

122999932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496778-G-A

123000115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496605-A-T

123000136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496575-G-T

123000240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496472-G-A

123000265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496450-A-G

123000346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496395-T-C

123000405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496338-C-T

123000555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496193-G-A

123000720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33496015-A-G

http://identifiers.org/hco/6/GRCh38#123000847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33495913-A-C

123000871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495892-A-G

123000967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495797-C-G

http://identifiers.org/hco/6/GRCh38#123001057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33495731-C-A

123001068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495720-G-T

http://identifiers.org/hco/6/GRCh38#123001259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33495534-C-A

123001335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495466-T-A

123001398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495414-T-A

123001590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495218-A-T

123001645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495173-G-A

123001645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495173-G-T

123001665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495152-T-G

123001699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33495118-A-G

123002554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33494232-A-G

123002692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33494111-A-G

123002813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33494013-C-T

123003057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493793-A-T

123003106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493744-A-T

123003311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493548-C-T

123003419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493440-A-G

123003535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493336-T-C

123003548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493323-A-T

123003658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493213-G-T

123003759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33493109-G-T

123003929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492901-A-G

123003945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492885-A-G

123004046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492822-T-G

123004118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492742-A-G

123004142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492721-G-T

123004144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492719-C-T

http://identifiers.org/hco/6/GRCh38#123004153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33492710-A-C

123004179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492689-C-G

123004280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492599-T-G

123004289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492593-G-A

123004289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492593-G-T

123004462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33492437-C-T

123005257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491989-T-G

http://identifiers.org/hco/6/GRCh38#123005342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33491906-C-A

123005342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491906-C-T

123005523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491724-A-T

123005852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491392-T-C

123005881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491358-G-T

123006092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491146-A-G

123006163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33491083-G-A

http://identifiers.org/hco/6/GRCh38#123006247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33491008-A-C

123006337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490908-G-A

123006537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490731-G-C

123006537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490731-G-T

123006700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490569-C-T

123006755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490514-T-C

123006825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490443-C-T

123006986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490282-C-T

123007128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33490163-G-T

http://identifiers.org/hco/6/GRCh38#123007308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33489985-A-C

123007308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489985-A-G

123007317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489977-G-A

http://identifiers.org/hco/6/GRCh38#123007388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33489908-C-A

123007404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489894-A-G

123007621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489525-T-C

123007638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489508-T-C

http://identifiers.org/hco/6/GRCh38#123007795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33489367-A-C

123008008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489151-C-T

123008059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489100-G-C

123008144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33489024-T-C

123008173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33488994-T-C

123008335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33488831-T-A

123008594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33488410-A-G

123008704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33488302-G-T

123008765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33488239-G-A

123008905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33488109-T-G

123010555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472655-T-G

123010772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472419-C-G

http://identifiers.org/hco/6/GRCh38#123010785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33472406-C-A

123010785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472406-C-T

123010791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472400-A-T

123010794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472397-T-C

123010842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472122-C-T

123010853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472111-T-G

http://identifiers.org/hco/6/GRCh38#123010871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33472096-C-A

123010910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472056-G-A

123010910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33472056-G-T

123010926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471974-T-G

123010974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471923-G-A

http://identifiers.org/hco/6/GRCh38#123011178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33471720-C-A

123011178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471720-C-T

123011219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471677-G-A

123011219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471677-G-T

123011237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471670-G-A

123011237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471670-G-T

123011252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471655-T-A

123011292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33471610-A-G

123011461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470936-G-A

123011484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470901-G-A

123011757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470624-A-G

123011909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470474-G-A

123011951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470421-C-G

123011952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470420-C-G

123011976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470296-T-C

http://identifiers.org/hco/6/GRCh38#123012202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33470068-C-A

123012202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470068-C-G

123012202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33470068-C-T

123012305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469981-G-A

123012305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469981-G-C

123012318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469968-T-C

123012398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469891-G-A

http://identifiers.org/hco/6/GRCh38#123012643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33469502-C-A

123012672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469467-G-C

123012706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469434-G-A

123012770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33469373-G-A

http://identifiers.org/hco/6/GRCh38#123012785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33469358-C-A

123013341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33468157-C-T

123013400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33468094-A-T

123013442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33468054-T-C

123013567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467928-G-C

http://identifiers.org/hco/6/GRCh38#123013615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33467880-C-A

123014422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467781-A-T

123014460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467743-A-G

123014507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467696-G-A

123014680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467538-G-A

123014782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467397-A-G

123015006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467166-G-C

http://identifiers.org/hco/6/GRCh38#123015023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33467149-A-C

123015046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467127-T-C

123015127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33467052-A-G

123015198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466991-C-G

123015414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466779-T-C

123015602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466610-A-G

123015628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466598-T-A

123015646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466580-G-A

123015769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466460-T-A

http://identifiers.org/hco/6/GRCh38#123015810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33466422-C-A

http://identifiers.org/hco/6/GRCh38#123015874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33466361-A-C

123016183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33466134-A-G

123016412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465952-G-A

123016412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465952-G-T

123016490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465868-A-G

123016556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465803-C-T

123016564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465795-T-C

123016789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465589-C-G

123016858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465543-T-C

123016897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465496-C-G

123016905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465488-T-G

123017088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465310-A-G

123017120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465297-A-G

123017120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465297-A-T

123017397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465045-G-A

123017397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33465045-G-C

123017491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464953-T-A

123017655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464789-T-C

123017667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464780-A-G

123017986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464437-T-C

123017986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464437-T-G

123018010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464413-T-A

123018010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464413-T-C

123018087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464338-G-T

123018123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33464302-A-G

123018595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33462298-T-A

123018647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33462246-T-C

123018997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33461904-C-T

123019116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33461773-T-C

123022611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33458264-C-G

123022611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33458264-C-T

123026693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33455001-C-G

123026780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33454918-T-A

123026780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33454918-T-C

123026943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33448088-A-G

123027074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33447949-G-A

123027092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33447931-G-A

123027132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33447891-A-G

123027422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33447160-T-G

123027542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33447039-C-T

123027548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33447033-G-T

123027850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33446787-G-A

123027850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33446787-G-T

123027957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33446677-A-G

123027995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33445572-C-T

123028050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33445518-G-T

123028115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33445486-T-C

123028153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33445448-C-T

123029356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33437077-G-A

123029440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33436988-T-C

123029842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33435096-T-C

123029893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33435043-C-T

123029894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33435042-G-A

123029902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33435034-A-G

123029907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33435029-T-G

123030107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33434621-C-T

123030139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33434589-C-T

123030184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33434544-G-A

123030547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33434217-T-C

123031957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33432818-G-C

123031962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33432813-A-G

http://identifiers.org/hco/6/GRCh38#123035083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33429689-A-C

123035083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33429689-A-G

http://identifiers.org/hco/6/GRCh38#123035198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33429575-A-C

123038758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33427675-T-C

123038797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33427629-T-C

http://identifiers.org/hco/6/GRCh38#123038940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33427452-C-A

http://identifiers.org/hco/6/GRCh38#123039142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33427290-C-A

123039285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33427167-T-C

http://identifiers.org/hco/6/GRCh38#123039630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33426894-C-A

123040422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33426667-T-C

123040439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33426648-G-A

123040444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33426642-G-A

123041624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33426114-A-G

123042044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33424138-A-G

123042049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33424133-G-T

123042062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33424120-T-G

123042188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33423150-A-T

123042389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422682-G-A

123042632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422440-A-G

123042886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422212-A-G

http://identifiers.org/hco/6/GRCh38#123042928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33422179-C-A

123042928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422179-C-T

123043038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422069-G-A

123043038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422069-G-C

123043038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33422069-G-T

http://identifiers.org/hco/6/GRCh38#123047769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33420616-A-C

123047769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33420616-A-G

123047848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33420541-C-G

123047877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33420514-T-A

123048198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419887-T-C

123048337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419730-G-T

123048380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419690-A-G

123048433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419637-C-T

123048584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419521-A-G

123048597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419508-T-C

123048597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419508-T-G

123048612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419493-G-T

http://identifiers.org/hco/6/GRCh38#123048743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33419362-C-A

123048761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419344-T-C

http://identifiers.org/hco/6/GRCh38#123048771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33419334-C-A

123048872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419229-T-C

123048872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419229-T-G

123049007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33419118-A-G

123049178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418954-G-A

123049296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418858-G-A

123049296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418858-G-C

123049296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418858-G-T

123049379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418763-G-C

123049972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418241-C-T

123050000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418214-G-A

123050000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418214-G-T

123050027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33418199-T-A

123050504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33417749-T-C

123050564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33417688-A-G

http://identifiers.org/hco/6/GRCh38#123050638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33417633-C-A

123051075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33417204-A-G

123051196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33417085-A-G

123051210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33417072-T-A

123054024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416491-G-A

123054053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416462-C-G

123054082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416453-C-T

123054287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416244-G-A

123054289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416242-T-G

123054307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416224-T-G

123054326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416204-C-G

123054469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33416046-T-G

http://identifiers.org/hco/6/GRCh38#123054523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33415994-C-A

123054536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33415977-A-G

123054546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33415967-G-A

123054546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33415967-G-T

123055100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33405217-C-T

123055168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33405147-T-C

http://identifiers.org/hco/6/GRCh38#123055214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33405102-A-C

123055214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33405102-A-G

123055659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33404686-T-C

123055723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33404621-T-A

123055758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33404586-T-A

http://identifiers.org/hco/6/GRCh38#123055785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33404558-C-A

123055785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33404558-C-T

123055929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, missense_variant
orthologous variants: 33404414-G-A

123055959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, missense_variant
orthologous variants: 33404384-A-G

123055975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, missense_variant
orthologous variants: 33404368-G-C

123056049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33404294-A-G

123056049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33404294-A-T

123057029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, undefined
orthologous variants: 33395921-C-T

123057305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, undefined
orthologous variants: 33395680-T-C

123057325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33395659-G-A

123057358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33395626-T-A

123057384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33395613-T-A

123057384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33395613-T-C

123057825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33395371-C-G

123058182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33395048-C-T

123058285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33394936-A-G

http://identifiers.org/hco/6/GRCh38#123062766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33392056-C-A

123063253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389744-T-C

123063300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389709-T-G

123063328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389685-A-G

123063440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389572-T-C

123063561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389485-T-G

123063562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389484-A-T

http://identifiers.org/hco/6/GRCh38#123063584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33389462-C-A

123063595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389440-T-C

123063618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389394-G-A

123063618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389394-G-C

123063629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389384-A-G

123063651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389363-G-A

123063651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: intron variant
orthologous variants: 33389363-G-T

123063804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389210-T-C

123063807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389207-G-A

123063925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389094-G-A

123063925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389094-G-C

123063925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389094-G-T

123063992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389028-T-A

123063992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389028-T-C

123063992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33389028-T-G

123064099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388923-A-G

123064284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388736-A-G

http://identifiers.org/hco/6/GRCh38#123064374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33388647-C-A

123064374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388647-C-G

123064454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388564-G-A

123064466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388530-A-G

123064475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388521-C-T

http://identifiers.org/hco/6/GRCh38#123064480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33388516-C-A

123064507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388490-T-A

123064569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388440-G-T

123064654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388360-G-A

123064654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388360-G-T

123064666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388348-A-G

123064729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388289-T-G

123064904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23046
most severe consequence: 3 prime UTR variant
orthologous variants: 33388163-T-C