17630897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3 prime UTR variant
orthologous variants: 45687072-T-C

17631150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687269-G-T

17631194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687316-C-T

17631195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687317-A-G

17631485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45687342-G-T

17631796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45687635-C-T

17631810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45687649-A-G

17631857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45687718-T-C

17632392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687940-A-G

17632392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687940-A-T

17632405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687953-G-A

17632405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687953-G-T

http://identifiers.org/hco/4/GRCh38#17632416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#45687968-C-A

17632416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 45687968-C-T

17632474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3 prime UTR variant
orthologous variants: 45688029-G-A

17632474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3 prime UTR variant
orthologous variants: 45688029-G-T

17632629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 45688176-A-G

http://identifiers.org/hco/4/GRCh38#17632640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45688187-A-C

17632643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45688190-T-C

17632643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45688190-T-G

17632650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45688197-A-G

17632702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45688248-G-A

17632702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45688248-G-T

http://identifiers.org/hco/4/GRCh38#17632739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45688277-C-A

17632739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45688277-C-G

17633411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45688812-G-A

17633411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45688812-G-T

17633461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45688857-A-G

17633492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45688882-A-G

http://identifiers.org/hco/4/GRCh38#17633515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45688909-C-A

17633515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 45688909-C-T

http://identifiers.org/hco/4/GRCh38#17633516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45688910-C-A

http://identifiers.org/hco/4/GRCh38#17633590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45688994-C-A

http://identifiers.org/hco/4/GRCh38#17633623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45689043-A-C

http://identifiers.org/hco/4/GRCh38#17633706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45689117-A-C

17633826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 45689237-T-C

17633911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45689324-T-G

17634012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45689414-A-G

17634023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45689425-T-A

http://identifiers.org/hco/4/GRCh38#17634936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45690006-C-A

17634936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690006-C-G

17634936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690006-C-T

http://identifiers.org/hco/4/GRCh38#17634937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45690007-C-A

17634937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690007-C-T

17634954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690029-A-G

17634954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690029-A-T

17635117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45690181-G-C

17635130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690194-A-G

17635145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690209-G-C

17635145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690209-G-T

17635174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690238-G-T

http://identifiers.org/hco/4/GRCh38#17635245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45690302-A-C

http://identifiers.org/hco/4/GRCh38#17635248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45690305-C-A

17635248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690305-C-T

http://identifiers.org/hco/4/GRCh38#17635251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45690308-C-A

17635251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690308-C-T

17635267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690324-T-C

17635460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690539-C-G

17635676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45690984-A-T

17635705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691008-T-C

17635887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691186-A-T

17636074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691372-T-A

http://identifiers.org/hco/4/GRCh38#17636431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45691438-C-A

17636431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691438-C-T

http://identifiers.org/hco/4/GRCh38#17636459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45691467-A-C

17636459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691467-A-G

17636492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691484-C-G

17636492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691484-C-T

http://identifiers.org/hco/4/GRCh38#17636493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45691485-A-C

17636493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691485-A-G

17636546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45691513-G-T

17636552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45691519-T-C

17636567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45691534-G-C

17636567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45691534-G-T

17636594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45691561-G-T

17636618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45691585-C-G

17636635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45691602-A-T

http://identifiers.org/hco/4/GRCh38#17636656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45691623-C-A

17636656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691623-C-T

http://identifiers.org/hco/4/GRCh38#17636681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45691639-C-A

17636681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691639-C-G

17636681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691639-C-T

17636698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691656-A-G

17636698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691656-A-T

17636721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691661-T-A

17636721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691661-T-C

http://identifiers.org/hco/4/GRCh38#17636812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45691714-C-A

17636908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45691769-G-A

17639395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 45695076-A-G

17639472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695152-C-G

17639472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695152-C-T

17639504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695172-G-T

17639516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695184-G-T

http://identifiers.org/hco/4/GRCh38#17639519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45695187-C-A

17639519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695187-C-G

17639519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695187-C-T

17639534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695193-G-A

17639535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695194-G-C

17639535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695194-G-T

http://identifiers.org/hco/4/GRCh38#17639536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45695195-A-C

17639543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45695202-G-A

17642139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45697081-C-T

17642154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45697096-G-C

17642154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45697096-G-T

http://identifiers.org/hco/4/GRCh38#17642203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45697127-C-A

17642203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45697127-C-T

http://identifiers.org/hco/4/GRCh38#17642208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45697132-C-A

17642208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45697132-C-T

17642231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45697155-G-A

17642231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45697155-G-C

17642231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45697155-G-T

17646865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45697764-G-A

17646865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45697764-G-T

17646883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45697782-G-A

17646928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45697836-G-A

http://identifiers.org/hco/4/GRCh38#17646997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45697886-C-A

17647013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45697897-G-A

17647092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45697959-G-A

http://identifiers.org/hco/4/GRCh38#17647148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45698013-A-C

17647554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698103-G-A

17647554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698103-G-T

17647559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698108-T-A

17647559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698108-T-C

17647588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698136-G-T

17647589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698137-A-T

17647594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698142-G-A

17647594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698142-G-T

17647621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698169-G-C

17647621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698169-G-T

17647668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45698215-C-G

17647684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45698231-T-C

17647723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45698279-G-A

17647790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 45698346-C-T

17647879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698417-G-A

17647879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698417-G-C

17647879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698417-G-T

17647912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698450-G-A

17647912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698450-G-T

17647914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698452-T-A

17647917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698455-G-T

17647970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698471-C-T

17648083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45698539-G-A

17648112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45698567-G-T

17648196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45698655-G-A

17648278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45698739-T-C

17648287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698748-C-T

17648306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45698766-G-A

17648722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698869-T-C

17648727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698874-G-C

17648727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45698874-G-T

17652755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45699496-T-C

17652842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45699581-C-T

17652924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45699663-T-A

17652924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45699663-T-C

17652951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45699678-G-A

17653013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45699731-T-C

17653021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45699735-G-C

17653021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45699735-G-T

http://identifiers.org/hco/4/GRCh38#17653087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45699750-C-A

17653087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45699750-C-T

17656888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45707157-A-G

17657055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45707312-T-A

17657443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45707625-G-A

17658041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708086-C-T

17658106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708241-G-A

17658180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708286-A-T

http://identifiers.org/hco/4/GRCh38#17658204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45708308-C-A

17658204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708308-C-T

17658256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708344-T-C

17658256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708344-T-G

http://identifiers.org/hco/4/GRCh38#17658279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45708360-C-A

17658279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708360-C-T

17658293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708369-G-A

17658293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708369-G-T

17658296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708372-G-A

17658296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708372-G-T

17658297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708373-T-C

17658367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45708439-T-C

http://identifiers.org/hco/4/GRCh38#17658391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45708463-C-A

17658391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45708463-C-G

17658467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45708533-C-T

17658477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45708542-T-G

17658514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45708579-C-T

17658604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708668-T-C

http://identifiers.org/hco/4/GRCh38#17658667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45708731-C-A

17658667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45708731-C-T

http://identifiers.org/hco/4/GRCh38#17658739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45708815-C-A

http://identifiers.org/hco/4/GRCh38#17659818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45710277-C-A

http://identifiers.org/hco/4/GRCh38#17659830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45710289-C-A

17659833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710292-T-C

17659841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710300-T-G

http://identifiers.org/hco/4/GRCh38#17659860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45710318-C-A

17659860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710318-C-T

17660018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45710482-T-A

17660018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45710482-T-C

17660049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45710513-G-A

17660189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710626-C-T

17660473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710821-T-C

17660473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710821-T-G

17660538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710888-T-C

17660558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45710908-G-A

http://identifiers.org/hco/4/GRCh38#17660640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45710977-A-C

17660778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45711093-G-A

17664343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712133-A-T

17664423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712311-G-A

17664423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712311-G-T

17664482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712365-G-T

17664497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712380-T-C

17664537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712418-C-T

17664544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712422-C-G

17664552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712430-C-T

17664700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712553-G-A

17664700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712553-G-T

17664708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712561-T-A

17664708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712561-T-G

17664876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712701-G-A

17664921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45712742-A-G

17664952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45712771-C-T

http://identifiers.org/hco/4/GRCh38#17665051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#45712867-C-A

17665051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: 45712867-C-G

17665301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45713114-A-G

17665311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45713124-T-A

17665610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45713437-G-A

17665805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45713627-G-C

17665819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45713641-G-A

17680562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45716180-G-A

17680691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45716326-C-T

17680760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45716388-C-T

17680869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45716475-C-T

17681252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45716848-G-A

17681477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717077-G-A

17681625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717197-A-G

http://identifiers.org/hco/4/GRCh38#17681674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45717230-C-A

17681674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717230-C-T

http://identifiers.org/hco/4/GRCh38#17681735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45717285-C-A

17681805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717354-G-A

17681805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717354-G-C

17681999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717581-C-G

17681999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717581-C-T

http://identifiers.org/hco/4/GRCh38#17682033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45717614-A-C

17682035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717616-A-G

17682207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717772-C-T

17682298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45717854-G-A

http://identifiers.org/hco/4/GRCh38#17682894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45718091-C-A

http://identifiers.org/hco/4/GRCh38#17682939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45718136-C-A

17682939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718136-C-T

17683021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718198-C-T

17683298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718466-G-A

17683306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718474-C-T

17683328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718496-G-A

17683443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718595-T-C

17683529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718680-G-A

17683657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45718791-T-A

17684203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: -A-T

17684323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: -A-G

17684476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: -A-G

17684479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: -A-G

17684605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: -C-T

17684693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: -G-A

17685590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719480-T-G

17685629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719518-G-A

17685642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719531-C-T

17685681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719570-A-G

http://identifiers.org/hco/4/GRCh38#17685699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45719587-C-A

17685699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719587-C-T

17685724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719630-G-C

17685740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719646-C-T

17685781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719676-C-T

http://identifiers.org/hco/4/GRCh38#17685820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45719703-A-C

17685933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719827-T-G

17685965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719863-G-A

17686045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45719935-G-T

17686313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45720196-T-G

http://identifiers.org/hco/4/GRCh38#17686327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45720210-C-A

17686327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45720210-C-G

17686327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45720210-C-T

17686361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45720244-A-G

17687189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45722822-C-T

http://identifiers.org/hco/4/GRCh38#17687227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45722787-C-A

17687864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721611-T-G

17687903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721573-C-T

17687970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721511-T-G

17687978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721503-C-T

17688113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721395-A-G

17688114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721394-T-A

17688209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721312-T-G

17688302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721221-G-A

17688302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721221-G-T

17688404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45721119-C-T

http://identifiers.org/hco/4/GRCh38#17688470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45721053-C-A

17688470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45721053-C-T

17688486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45721037-T-C

17689110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45720761-A-G

17689327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45723461-C-T

17690826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45725675-C-T

17690870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45725718-G-A

http://identifiers.org/hco/4/GRCh38#17691092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45726329-C-A

17691092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45726329-C-G

http://identifiers.org/hco/4/GRCh38#17691175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45726397-C-A

17691175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45726397-C-T

17691329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45726557-C-T

17691363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45726588-C-T

17692812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730058-C-T

17692847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730080-G-T

17693183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730411-G-T

17693196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730424-G-A

17693196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730424-G-T

17693326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45730570-C-T

17693398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45730642-C-T

17693423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730667-A-G

http://identifiers.org/hco/4/GRCh38#17693438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45730682-C-A

17693443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730687-A-G

17693473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730716-C-T

17693493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730739-G-T

http://identifiers.org/hco/4/GRCh38#17693498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45730744-C-A

17693498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730744-C-G

17693518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730760-A-G

17693558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730799-A-G

17694017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45730998-C-T

17694087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45731064-C-T

17694098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45731072-C-G

17694098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45731072-C-T

17694760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45731385-C-T

17694818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45731442-A-G

17696865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733187-G-A

17696886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733207-A-G

17697074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733360-T-C

17697158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733444-G-C

17697216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733500-T-A

17697216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733500-T-C

http://identifiers.org/hco/4/GRCh38#17697295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45733576-C-A

17697362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733647-G-A

17697371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733656-T-A

17697420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733877-T-A

17697425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45733890-A-G

17697997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734458-A-G

17698029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734473-G-A

17698040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734482-G-A

http://identifiers.org/hco/4/GRCh38#17698048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45734490-C-A

17698048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734490-C-T

17698070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734518-G-T

17698336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734738-C-T

17698393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734795-G-C

17698426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45734828-G-A

17702210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45735868-C-T

17702316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45735975-A-T

17702539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45736195-T-C

http://identifiers.org/hco/4/GRCh38#17702804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45736440-C-A

17702965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45736567-G-A

17702997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45736597-G-T

17703167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45736738-T-C

17704002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45736916-A-G

17704261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45737260-A-G

17704595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45737507-G-C

17704836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45737709-T-C

17704922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45737795-G-A

17704935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45737808-A-G

http://identifiers.org/hco/4/GRCh38#17704969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45737842-C-A

17704992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45737858-G-A

17705176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45738039-A-G

17705238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738104-C-T

17705247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738113-G-T

17705248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738114-G-A

17705248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738114-G-T

17705300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738143-T-A

17705300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738143-T-C

17705300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738143-T-G

http://identifiers.org/hco/4/GRCh38#17705323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45738166-C-A

17705324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738167-A-T

17705350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738193-T-A

17705350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738193-T-C

17705405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738261-G-A

17705550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738378-G-A

17705634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738503-G-A

17705634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738503-G-T

17705643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738508-G-T

17705655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738563-A-T

17705663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738571-T-C

17705728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738758-C-G

17705728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45738758-C-T

http://identifiers.org/hco/4/GRCh38#17705736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45738770-C-A

17705779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45738882-A-G

http://identifiers.org/hco/4/GRCh38#17705987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45739082-C-A

17706018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739113-G-A

17706018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739113-G-T

17706026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739121-G-A

17706026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739121-G-C

17706026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739121-G-T

http://identifiers.org/hco/4/GRCh38#17706036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45739130-C-A

17706036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739130-C-T

http://identifiers.org/hco/4/GRCh38#17706057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45739172-C-A

17706147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739257-G-A

http://identifiers.org/hco/4/GRCh38#17706179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45739291-C-A

17706317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739435-C-T

17706482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739599-G-A

17706482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739599-G-T

17707285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739819-A-G

17707329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739862-G-A

17707415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739926-T-C

17707466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45739975-G-A

17707501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740005-G-T

17707504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740008-A-G

17707504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740008-A-T

17707505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740009-T-C

17707524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740028-A-G

17707526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740029-G-T

17707528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740031-C-T

17707543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740046-T-A

17707543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740046-T-C

17707607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740103-T-G

http://identifiers.org/hco/4/GRCh38#17707663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45740157-C-A

17707663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45740157-C-T

http://identifiers.org/hco/4/GRCh38#17707700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45740194-C-A

17707700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45740194-C-T

17707731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45740225-G-C

17707746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45740240-A-G

17707746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45740240-A-T

17707863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45740340-G-T

17708180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741012-C-G

17708215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741042-T-C

17708296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741115-C-T

17708305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741124-T-C

17708357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741176-T-C

17708761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741199-T-A

17708838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45741277-A-G

17708995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741427-G-A

17708995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741427-G-T

17709012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741444-G-A

17709015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741447-G-T

17709018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741450-C-G

17709030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741462-C-G

17709030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741462-C-T

17709039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741471-C-G

17709231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741663-C-G

17709243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741675-A-G

17709256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741688-G-T

17709258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741690-C-T

17709282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741714-G-A

17709282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741714-G-C

17709296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741728-G-C

17709426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous_variant, undefined
orthologous variants: 45741858-A-T

http://identifiers.org/hco/4/GRCh38#17709456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45741888-C-A

17709456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45741888-C-T

17709500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45741932-C-T

17709604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: missense variant
orthologous variants: 45742042-G-T

17709612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45742050-C-T

http://identifiers.org/hco/4/GRCh38#17709655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45742093-A-C

17709655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742093-A-G

17709699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742140-G-A

17709699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742140-G-T

http://identifiers.org/hco/4/GRCh38#17709724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45742168-C-A

17709724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742168-C-G

17709724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742168-C-T

17709748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742192-G-T

17709780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742224-G-T

17709795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742245-G-A

17709795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742245-G-T

17709887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742334-A-G

17709889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742336-A-G

17710594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45742832-T-C

17711083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45743410-T-C

17713338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45744240-T-C

http://identifiers.org/hco/4/GRCh38#17713579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45744483-A-C

17713611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45744514-C-T

17714079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45746149-A-G

17714133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45746203-G-A

17714183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45746255-C-T

17714263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45746336-G-A

17714740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45748210-G-A

17714928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45748398-A-T

17716021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45748535-C-T

17719823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45751320-C-T

17720075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45751546-G-A

17720290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45751758-A-G

17720388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45751856-A-G

17720531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45751998-A-G

17722199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45752944-G-A

17722302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45753049-G-A

17722951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45753664-A-T

17723115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45754590-T-C

17723289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45755577-G-A

http://identifiers.org/hco/4/GRCh38#17723586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45755824-C-A

17723594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45755832-T-G

17723710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45755910-G-C

17723717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45755913-G-T

17724062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45755986-C-T

17724237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45756132-G-C

17724389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45756277-G-A

17724484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45756373-G-A

http://identifiers.org/hco/4/GRCh38#17724860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45756725-C-A

17724860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45756725-C-T

17725084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45756909-G-T

17725268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757118-G-C

17735832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757478-T-C

17735842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757487-C-T

17735965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757595-C-T

17735977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757607-A-G

17736177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757806-G-A

17736190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757818-G-A

17736316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757877-A-G

17736339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757900-T-A

17736375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45757909-T-C

http://identifiers.org/hco/4/GRCh38#17736599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45758133-C-A

17736699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45758226-G-A

17736724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45758249-C-T

17736753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45758278-T-C

http://identifiers.org/hco/4/GRCh38#17737492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45758668-A-C

http://identifiers.org/hco/4/GRCh38#17737576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45758735-A-C

17737576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45758735-A-G

17737688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45758891-C-T

http://identifiers.org/hco/4/GRCh38#17737755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45758951-C-A

17738246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45759419-A-T

17738444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45759612-A-T

17738500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45759665-A-G

17738500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45759665-A-T

17739020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45759907-T-G

17739105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45759954-C-G

17739427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45760238-G-A

17739434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45760245-C-G

17739447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45760258-C-T

17739491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45760305-G-C

17739509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45760322-A-T

17741160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45760827-A-G

17743736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45767410-G-A

17743874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45767579-G-A

17744313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45767972-T-C

17744380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45768041-G-A

17744633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45768139-T-C

17744633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45768139-T-G

17744880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45768266-A-G

17744880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45768266-A-T

17745184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45770640-C-G

17745452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45770858-C-T

http://identifiers.org/hco/4/GRCh38#17745468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45770874-A-C

17745514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45770917-C-T

17745554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45770952-G-C

17745629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771028-C-T

17745672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771049-T-C

17745814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771191-C-G

17747185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771785-T-C

17747226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771822-G-A

17747226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771822-G-C

17747276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771871-G-A

17747394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771981-C-G

17747405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45771992-G-A

17747424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772010-A-T

17747435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772021-G-A

17747452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772038-T-C

17747461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772047-G-A

17748161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772128-T-C

17748196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772177-C-T

17748208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772189-T-C

17748230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772211-A-T

17748506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45772439-T-G

17749962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773216-C-T

17749963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773217-A-G

17750032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773289-T-C

17750095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773345-T-C

17750107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773357-C-T

17750139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773390-G-A

17750209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773465-C-T

17750241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773497-C-T

17750248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773508-C-T

17750312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773568-G-A

17750399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45773655-T-C

17750616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774120-T-C

17750803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774300-C-T

17750878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774362-T-A

17750888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774372-C-T

17750933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774413-C-T

17750936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774416-G-A

17752186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45774900-C-T

17752400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45775101-T-A

17752452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45775155-T-C

http://identifiers.org/hco/4/GRCh38#17752702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45776056-C-A

17752729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45776083-G-A

17758166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45778397-T-C

17758211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45778448-C-T

17758261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45778528-C-T

17758265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45778532-A-T

http://identifiers.org/hco/4/GRCh38#17758554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45778748-C-A

http://identifiers.org/hco/4/GRCh38#17758756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45778913-A-C

http://identifiers.org/hco/4/GRCh38#17758884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45779285-C-A

17758884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45779285-C-G

17759034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45779434-C-T

17759047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45779447-C-T

17759117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45779517-C-T

17759171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45779558-T-A

17760866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45780391-A-G

17760952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45780478-C-T

17761022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45780584-A-G

17761027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45780589-T-C

17761290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45783286-T-C

17761444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45783421-T-C

17761505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45783481-C-G

17761830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45783560-G-C

17761853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45783583-C-T

17761978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45783704-G-A

17762619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45784304-A-T

17762969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45784577-G-A

17763078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45784664-T-C

http://identifiers.org/hco/4/GRCh38#17763746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45785391-C-A

17763746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45785391-C-T

17763826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45785471-T-C

17764327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45785948-G-A

17764327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45785948-G-C

17764748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45786415-A-G

17765148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45788440-G-A

17765148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45788440-G-T

17765596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45788888-T-G

17770055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45789640-T-A

17770070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45789654-G-A

17770070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45789654-G-T

17770126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45789705-A-G

http://identifiers.org/hco/4/GRCh38#17771208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#45790766-A-C

17771430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45790964-G-A

17771430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45790964-G-T

http://identifiers.org/hco/4/GRCh38#17771771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45791293-C-A

17778934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45793716-T-A

17779002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45793774-C-G

17779002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45793774-C-T

17779126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45793898-G-A

17779300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45794043-A-G

17779451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45794193-T-G

17779586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45794326-C-T

http://identifiers.org/hco/4/GRCh38#17779723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#45795029-C-A

17779800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45795102-A-G

17780107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45795380-G-A

17780215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45795459-G-C

17780889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45796175-C-T

17781026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45796309-C-T

17781082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45796356-G-A

17781082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: intron variant
orthologous variants: 45796356-G-C

17781219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: synonymous variant
orthologous variants: 45796495-T-C

17781399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 5 prime UTR variant
orthologous variants: 45796680-G-C

17781435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45796713-G-A

17781435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45796713-G-T

17781557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45796830-G-A

17781557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45796830-G-C

17781557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29235
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45796830-G-T