39743090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336013-T-C

39743121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336037-A-G

39743230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336138-G-C

39743230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336138-G-T

39743307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336200-G-C

39743307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336200-G-T

http://identifiers.org/hco/22/GRCh38#39743380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80336283-C-A

39743380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336283-C-T

39743405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336308-A-G

39743459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: 80336371-A-G

http://identifiers.org/hco/22/GRCh38#39743479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80336391-C-A

39743767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336664-A-G

39743801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336698-T-C

39743801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336698-T-G

39743826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80336723-G-A

39743858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336755-T-C

39743877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80336771-A-G

39743911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336805-C-G

39743986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336886-C-G

39744008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336908-C-G

39744059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80336941-C-T

39744171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80337053-A-G

39744171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80337053-A-T

39744263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, missense_variant
orthologous variants: 80337145-C-G

39744343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80337218-A-G

39744402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80337268-G-T

39744496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80337360-T-C

39745219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80338497-T-C

39745253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80338532-T-C

http://identifiers.org/hco/22/GRCh38#39745299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80338578-C-A

39745299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80338578-C-G

39745319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80338596-T-C

http://identifiers.org/hco/22/GRCh38#39745608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80338887-C-A

39745609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80338888-A-G

39748627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80343827-G-A

39749124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80344375-C-T

39749287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80344528-C-T

39749543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80344779-T-A

39749543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80344779-T-C

39749698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80344904-T-C

39753403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80345982-G-C

39753512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80346066-T-C

39753779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80346273-G-C

39754039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80346516-T-G

39755338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80348037-G-T

39755515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80348195-C-T

39755565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80348254-C-T

39764817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80357922-C-T

39764853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80357944-C-T

39764863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80357954-T-G

39764890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80357985-T-C

39765104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358188-T-A

39765104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358188-T-G

39765119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358203-A-G

39765126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358205-G-A

39765128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358207-G-T

39765149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358225-A-G

39765165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358241-G-T

39765312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80358374-A-G

39765313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80358375-C-T

39765455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80358520-C-G

39765455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80358520-C-T

39765534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80358599-A-T

39765538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80358603-C-T

39765725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358752-T-A

39765966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80358992-C-T

39766067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80359033-T-A

39766304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80359205-G-T

39766441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80359342-T-A

39766971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80363200-A-G

http://identifiers.org/hco/22/GRCh38#39767583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80363639-C-A

39767697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80363738-A-G

39767784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80363828-A-T

39767950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364104-T-A

39767950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364104-T-C

39768154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364434-C-G

39768154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364434-C-T

39768206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364489-C-G

39768333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364590-T-A

39768333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80364590-T-C

http://identifiers.org/hco/22/GRCh38#39773937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80365287-C-A

39773937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80365287-C-T

39773978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80365323-G-C

39774045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80365391-G-T

39774365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, undefined
orthologous variants: 80365693-A-G

39774405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80365724-C-T

39774498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80365779-C-T

http://identifiers.org/hco/22/GRCh38#39774598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80365838-C-A

39774598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80365838-C-T

http://identifiers.org/hco/22/GRCh38#39774679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80365884-A-C

39774945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366025-T-C

39774985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366055-G-T

39775237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366329-T-C

39775282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366373-G-C

http://identifiers.org/hco/22/GRCh38#39775555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80366620-C-A

39775751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366789-T-C

39775752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366790-A-G

39776195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80366916-A-G

39776412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80367106-T-C

39776507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80367186-C-G

39776595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80367258-T-C

39777005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80367686-A-G

39777425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368120-G-T

39777426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368121-G-A

39777516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368188-A-G

39777518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368190-T-C

39777648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368288-A-G

39777736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368362-T-C

39777736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368362-T-G

39777822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368446-A-G

39778338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368895-G-C

39778366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80368922-T-C

39778503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80369058-C-T

39778525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80369080-T-C

http://identifiers.org/hco/22/GRCh38#39778582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80369136-A-C

39778589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80369140-A-G

39778686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80369230-C-G

39800622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80373898-T-C

39800744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374004-G-A

39800913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374129-C-T

39801033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374246-A-G

39801041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374254-C-T

http://identifiers.org/hco/22/GRCh38#39801167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80374379-C-A

39801197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374424-G-A

39801344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374555-C-T

39801447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374654-T-C

39801459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80374668-A-G

http://identifiers.org/hco/22/GRCh38#39801665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80375233-C-A

39801886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80375439-T-C

39801986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80375525-T-G

http://identifiers.org/hco/22/GRCh38#39803433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80376461-C-A

39803540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80376566-T-C

39804472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80376832-A-G

39805053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80377408-G-A

39805372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80377679-T-C

39805437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80377744-T-A

39805836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378065-C-T

39805992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378179-G-T

39806089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378265-C-T

39806215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378395-C-G

39806215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378395-C-T

39806244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378409-C-T

39806372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378531-T-C

39806492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378647-C-T

39806752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80378778-C-T

http://identifiers.org/hco/22/GRCh38#39806873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80378895-C-A

39807233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379093-G-A

http://identifiers.org/hco/22/GRCh38#39807325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80379195-C-A

39807387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379275-T-C

39807387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379275-T-G

39807498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379352-A-G

http://identifiers.org/hco/22/GRCh38#39807548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80379389-A-C

39807558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379399-A-G

39807571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379412-G-T

39808174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379776-G-A

39808174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379776-G-T

39808275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379876-C-T

39808329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80379926-G-A

39809201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80380970-T-C

39809224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80380992-C-T

39809364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80381104-A-G

39809378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80381118-C-G

39809506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80381231-A-G

39811525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80381562-C-T

39812455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382539-T-C

39812457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382541-T-C

39812458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382542-G-A

39812819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382719-G-A

39813009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382835-C-T

39813053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382866-G-A

39813185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382977-C-G

39813191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80382983-T-C

39814265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80384093-C-T

http://identifiers.org/hco/22/GRCh38#39814529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80384336-C-A

39814529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80384336-C-T

39814825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80384603-T-C

39814951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80384728-T-C

39815181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80384870-G-A

39815272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, undefined
orthologous variants: 80384927-G-A

39815523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80385039-G-A

http://identifiers.org/hco/22/GRCh38#39815527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80385043-A-C

39815563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80385062-C-G

39815570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80385069-G-C

39815573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80385072-T-C

39815602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80385100-C-T

39816347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80385573-A-G

39818825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80390548-C-G

39818825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80390548-C-T

http://identifiers.org/hco/22/GRCh38#39819936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80391703-A-C

39820684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80392946-G-A

39820692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80392954-T-C

39820700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80393042-C-G

39820810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80393168-T-G

http://identifiers.org/hco/22/GRCh38#39820902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80393254-C-A

39820902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80393254-C-T

39820957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, undefined
orthologous variants: 80393306-C-G

39827869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80397284-G-A

http://identifiers.org/hco/22/GRCh38#39828349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80396857-C-A

39828349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396857-C-T

39828374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396829-A-G

39828477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396730-G-A

39828597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396609-A-G

39828684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396517-A-T

39828686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396515-C-T

39828822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80396372-A-T

http://identifiers.org/hco/22/GRCh38#39835812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80398235-C-A

39835855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80398278-A-G

39835855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80398278-A-T

http://identifiers.org/hco/22/GRCh38#39835917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80398340-C-A

39835917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense variant
orthologous variants: 80398340-C-G

39835957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: missense_variant, splice_region_variant, synonymous_variant
orthologous variants: 80398380-T-A

39835957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 80398380-T-C

39835964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 80398387-A-G

39835967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80398390-A-G

39836063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80398467-T-C

39836094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80398502-A-G

39836094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80398502-A-T

39836141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80398535-G-C

39837585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80399540-G-A

39837673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80399713-T-C

39838553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80400833-G-C

http://identifiers.org/hco/22/GRCh38#39838794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80401119-A-C

39838794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80401119-A-G

39838826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80401153-A-G

http://identifiers.org/hco/22/GRCh38#39838859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80401186-A-C

39839073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80401791-A-G

39839548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80402110-C-T

39840008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80402905-T-C

39840011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80402908-C-T

39843862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80405671-G-A

39843862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80405671-G-C

39843972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80405771-T-G

39844694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80406358-A-G

39844790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80406447-C-T

39845181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80406683-C-T

39845814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80407315-A-G

39846066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80407570-T-A

39846066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80407570-T-C

39851544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80413093-T-C

39851728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80413285-C-T

39851912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80413438-G-A

39851912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80413438-G-T

39854330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414217-T-A

39854351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414238-T-C

http://identifiers.org/hco/22/GRCh38#39854352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80414239-A-C

39854729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414584-T-A

39854729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414584-T-G

39855098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414934-C-T

39855111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414947-C-G

39855118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80414954-C-T

39855225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415061-T-C

39855610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415409-A-G

39855611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415410-G-A

39855701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415496-A-G

39855805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415563-A-G

39855884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415616-G-C

39855951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80415681-A-G

http://identifiers.org/hco/22/GRCh38#39856539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80415972-A-C

39861647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80418586-A-G

39861672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80418612-T-A

39861679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80418619-T-C

39861679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80418619-T-G

http://identifiers.org/hco/22/GRCh38#39861748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80418683-A-C

39861748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80418683-A-G

39861800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, missense_variant
orthologous variants: 80418737-T-C

http://identifiers.org/hco/22/GRCh38#39861982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80418923-C-A

39861991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80418932-T-C

39862061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80419003-T-A

39864020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80419739-G-C

39864092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80419789-A-T

39864152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80419839-A-G

39864360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80419988-T-C

39864381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80419998-G-A

39864450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420073-T-G

39865006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420319-T-G

39865119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420428-C-T

39865167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420475-G-A

39865168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420476-T-A

39865342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420640-T-C

39865445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420726-G-A

39865445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420726-G-C

39865445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80420726-G-T

http://identifiers.org/hco/22/GRCh38#39867272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80422272-C-A

39867482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80422471-C-G

39867655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80422623-G-A

39868322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80423413-G-A

39868322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80423413-G-C

39868365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80423435-A-G

39868368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80423438-G-A

http://identifiers.org/hco/22/GRCh38#39868381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80423453-C-A

39871224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80429420-G-T

39871326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80429515-G-C

39871394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80429574-T-C

39871737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80429934-C-T

39872129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80430286-T-C

39872739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80431013-T-A

39873161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80431169-C-T

39873464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80431615-A-G

39873507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80431661-A-G

39873562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80431704-G-A

39882076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80436005-A-T

39882303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80436237-T-C

39882338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80436272-G-A

39883043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80436580-T-A

39883043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80436580-T-C

39885043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80441804-C-T

39885245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442007-T-C

39885245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442007-T-G

39885250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442012-A-G

39885505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442228-C-G

39885549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442272-T-C

39885551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442274-T-C

39886017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80442914-A-G

http://identifiers.org/hco/22/GRCh38#39886075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80443048-A-C

39886125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80443102-T-G

39886556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80443455-G-A

39887094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80443965-C-T

39887339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444157-G-A

39887339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444157-G-C

39887339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444157-G-T

39887350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444161-A-G

39887350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444161-A-T

39887476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80444281-C-T

39887557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: synonymous variant
orthologous variants: 80444362-A-G

http://identifiers.org/hco/22/GRCh38#39887605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80444410-A-C

39887719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80444524-A-G

http://identifiers.org/hco/22/GRCh38#39887787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80444595-C-A

39887824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80444626-T-C

39887840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80444639-G-T

39887885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80444683-T-C

39887893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80444691-G-A

39887893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80444691-G-T

39887933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444731-T-A

39887933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444731-T-C

39887982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444799-G-C

39888049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80444869-G-T

39889003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445208-C-T

39889052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445246-T-G

39889078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445269-C-G

39889079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445270-A-T

39889125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445304-T-C

39889290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445482-G-A

39889439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445637-G-A

39889478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445676-T-C

39889671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80445859-T-C

39890177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80446021-A-G

39890546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80446367-T-A

http://identifiers.org/hco/22/GRCh38#39890582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80446401-C-A

39890582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80446401-C-T

39890730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80446547-A-G

39891160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80447086-A-G

39891305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80447261-T-C

39891341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80447302-G-A

39892527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80447980-T-C

39892757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: intron variant
orthologous variants: 80448417-C-T

39893042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 80448708-C-T

39893228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80448846-A-G

39893254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80448868-A-G

39893292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80448908-G-T

http://identifiers.org/hco/22/GRCh38#39893388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80448991-C-A

http://identifiers.org/hco/22/GRCh38#39893416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80449011-C-A

39893416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80449011-C-T

http://identifiers.org/hco/22/GRCh38#39893444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80449040-C-A

39893469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80449070-G-A

39893469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80449070-G-T

39893503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80449101-A-G

39893503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80449101-A-T

39893514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449112-G-A

39893514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449112-G-T

39893515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449113-A-T

39893517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449115-G-T

39893530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449128-G-A

39893605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449162-G-A

39893605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80449162-G-T

http://identifiers.org/hco/22/GRCh38#39893741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#80449295-C-A

39893766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26352
most severe consequence: non coding transcript exon variant
orthologous variants: 80449319-G-T