http://identifiers.org/hco/10/GRCh38#101845717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45805913-C-A

101845759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45805964-A-G

101845806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806011-G-T

101845832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806027-T-C

101845833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806028-G-A

101845833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806028-G-C

101845893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806087-T-C

101845983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806159-A-G

101846033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806206-G-T

http://identifiers.org/hco/10/GRCh38#101846098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45806278-C-A

101846194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806369-A-G

101846360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806518-A-G

101846360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806518-A-T

101846402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806556-A-G

101846402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806556-A-T

101846437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806591-G-A

101846437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806591-G-T

101846634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806790-A-G

101846970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806834-A-G

101846970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806834-A-T

101847029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806882-G-A

101847048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806900-G-A

101847048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45806900-G-C

101847184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45807006-T-C

101847233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45807051-T-G

101847285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45807101-T-C

101847415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45807215-G-T

101848418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807546-G-A

101848455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807588-G-A

101848491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807616-G-A

101848705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807805-T-C

101849528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808478-G-A

101849604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808562-C-T

http://identifiers.org/hco/10/GRCh38#101849626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45808582-C-A

101849626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808582-C-T

http://identifiers.org/hco/10/GRCh38#101849676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45808628-C-A

101849682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808634-T-C

101849682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808634-T-G

101849703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808653-T-C

101849763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808700-G-A

101850309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809022-G-A

101850335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809039-G-T

101850516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809168-C-T

101850742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809247-C-T

101850747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809252-C-T

101851025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809475-T-C

101851115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809565-T-G

101851669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810264-G-A

101851903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810454-A-G

101851905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810456-C-T

101851962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45810509-G-A

101852114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45810644-C-G

http://identifiers.org/hco/10/GRCh38#101852236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45810763-C-A

101852236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45810763-C-G

101853258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810890-G-A

http://identifiers.org/hco/10/GRCh38#101853590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45811671-C-A

101853770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812082-T-C

101853776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812088-C-G

101853777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812089-C-G

101853910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812277-C-G

101853910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812277-C-T

101853919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812295-C-T

101853921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812297-T-A

101853921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812297-T-C

http://identifiers.org/hco/10/GRCh38#101854044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45812456-C-A

101854044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45812456-C-T

http://identifiers.org/hco/10/GRCh38#101854475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45812893-A-C

101854668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45813048-G-A

101854831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45813206-T-C

101854833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45813208-A-G

101854851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45813225-C-T

101858732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814545-G-A

101858787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814604-A-G

101858806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814625-T-G

101858898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814716-G-A

101858949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45814766-A-G

101859247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815126-T-A

101859380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815462-A-G

101859380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815462-A-T

101859396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815478-C-T

101859417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815494-G-A

101859613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45815655-A-G

101875327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45823310-T-C

101875399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45823382-G-T

101875554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45823548-C-G

101875631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45823625-G-A

101875692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45823686-A-G

101875961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45823947-T-C

101876480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45824439-C-T

101877808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45825023-T-C

101878980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45825499-C-G

101878980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45825499-C-T

101879645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45825787-C-T

101880017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45826116-C-T

101880058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45826157-G-C

101880375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45826450-A-G

101880439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45826516-C-T

101880693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45826776-C-G

101880838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45826897-T-C

101881889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45829946-C-T

101883623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830504-T-C

http://identifiers.org/hco/10/GRCh38#101884246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45830753-C-A

101884363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830925-T-A

101884369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45830931-T-C

101886821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831631-C-G

101886821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831631-C-T

101887039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45831861-T-G

101887311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832148-T-A

101887935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832528-T-C

101888326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832782-G-A

101888464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832924-C-G

101888539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45832997-T-C

http://identifiers.org/hco/10/GRCh38#101888793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45833785-C-A

101888793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833785-C-T

101888794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45833786-G-A

http://identifiers.org/hco/10/GRCh38#101888892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45833882-A-C

101889255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834386-A-G

http://identifiers.org/hco/10/GRCh38#101889314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45834446-C-A

101889314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834446-C-T

101889344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834486-C-T

101889383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45834517-T-C

101889534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45834669-G-A

http://identifiers.org/hco/10/GRCh38#101889760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45835546-A-C

http://identifiers.org/hco/10/GRCh38#101898452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45837396-C-A

101898452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45837396-C-G

101899890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45839965-G-A

101899890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45839965-G-C

101900191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45841662-T-A

101901221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45842829-T-C

101901509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45843123-T-C

101901789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45843379-A-G

101901899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45843453-T-A

101901925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45843476-T-C

101901939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45843490-A-T

101902034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45843558-G-A

101902420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45843922-T-G

101902582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844039-C-G

101902648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844104-C-T

101902745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844181-C-T

101902774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844210-T-C

101902786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844222-T-C

101902869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844304-T-C

101902906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844338-T-G

101903065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45844486-C-T

101903439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45845357-T-G

101903705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45845675-T-C

101903713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45845683-T-C

http://identifiers.org/hco/10/GRCh38#101903714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45845684-A-C

101904220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45847575-G-A

101904293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45847645-G-A

101904405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45847754-G-A

101904405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45847754-G-C

101904405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45847754-G-T

101904431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45847777-T-A

101905411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45849127-T-C

101906602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45849733-A-G

101906666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45849804-T-C

101906881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45850007-A-G

http://identifiers.org/hco/10/GRCh38#101906887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45850018-A-C

101907172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45850299-A-G

101907816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45851966-G-C

101913716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45852148-G-A

101913959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45852359-G-C

101914150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45852545-T-C

101916520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45854217-A-G

101917092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45854836-T-C

101917118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45854859-G-C

101917634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45855528-T-C

101917654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45855548-T-C

101917811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45855682-T-C

101917936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45855794-G-T

101918388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45855982-C-T

101918593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45856198-C-G

101918850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45856456-T-C

101918894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45856501-T-C

101919489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45857436-C-T

101919635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45857570-T-C

101919670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45857593-T-C

101920204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45858057-T-G

101922911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45859273-T-C

101924214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45860431-A-G

101924335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45860554-T-C

101927508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45861902-C-T

101928461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45862568-G-A

101929576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45863081-G-A

101930512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45865672-G-A

101930512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45865672-G-T

101930515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45865675-T-C

101931089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45866820-A-G

101933348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45869653-G-A

101933875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870053-T-C

101933899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870077-A-T

101933947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870112-T-C

101934020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870183-T-C

101934020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870183-T-G

101935397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870750-T-C

101935397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870750-T-G

101935485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870819-A-G

101935538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870866-T-C

101935624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45870947-A-T

101935967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871200-G-T

101936156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871342-G-C

101936322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871543-T-C

101936363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871567-G-A

101936369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871573-G-A

101936596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871769-G-A

101936596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871769-G-T

101936689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45871934-A-G

101937748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45872710-T-C

101937763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45872726-G-C

101938392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45873007-C-T

101938445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45873060-A-G

101938495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45873094-G-C

101938672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45873257-T-C

101939254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45873818-A-G

101939326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45873880-T-C

101939343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45873895-G-A

101939612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874148-G-A

101939741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45874273-T-C

101939819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874351-G-T

http://identifiers.org/hco/10/GRCh38#101939951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45874476-A-C

101939991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874514-A-G

101940025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874548-T-A

101940025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874548-T-C

http://identifiers.org/hco/10/GRCh38#101940041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45874564-C-A

101940041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874564-C-G

101940041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45874564-C-T

http://identifiers.org/hco/10/GRCh38#101940185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45874679-C-A

101940787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45875590-C-T

http://identifiers.org/hco/10/GRCh38#101940811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45875614-A-C

101940872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45875673-C-T

101940880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45875689-T-C

http://identifiers.org/hco/10/GRCh38#101956500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45879556-C-A

101956515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879568-G-C

101956515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879568-G-T

http://identifiers.org/hco/10/GRCh38#101956519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45879572-C-A

101956554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879600-A-G

101956592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879642-C-T

101956745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879794-A-G

101956789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879842-T-C

http://identifiers.org/hco/10/GRCh38#101956841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45879888-A-C

101956882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879923-T-C

101957009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45879978-A-G

101957165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880124-T-C

101957268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880211-C-T

101957283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880223-T-A

101957373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880332-C-G

101957373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880332-C-T

101957409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880363-T-A

101957577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45880431-T-C

http://identifiers.org/hco/10/GRCh38#101957713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45880568-C-A

101957713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45880568-C-G

101958093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45885604-C-T

101958121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45885632-A-G

101958855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45887367-T-C

101959026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45887516-C-T

101959235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45887730-G-A

101959293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45887797-C-G

101959545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45888277-T-C

101959553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45888285-T-C

101959574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45888306-C-T

101959593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45888325-G-C

101959669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45888395-T-A

101961312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890634-T-C

101961372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890690-G-C

101961672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890984-G-T

101961855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45891164-G-A

101962165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45891652-A-G

101962165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45891652-A-T

101965832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45899853-T-C

101965942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45899935-T-C

101966622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900094-C-T

101966657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900132-G-A

101966683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900165-T-G

101966861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900342-C-G

101966880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900360-G-C

101967364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900809-G-A

101967383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900832-A-G

101967415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900862-T-C

101967428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900875-C-T

101967857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45901162-T-C

http://identifiers.org/hco/10/GRCh38#101967972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45901223-C-A

101968423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902354-T-C

101968572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902517-G-C

101968678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902689-C-T

101968898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902939-C-T

101969044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45903289-G-A

101969044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45903289-G-C

101969683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904752-C-T

101970172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45905234-G-C

101970382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45905427-T-A

101970393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45905438-T-C

101970404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45905449-T-C

101971665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906139-A-G

101971689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906167-C-T

101971702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906179-T-C

101971704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906181-T-C

101972004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906454-G-C

101972121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45906564-A-G

101972363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45906793-G-A

101972363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45906793-G-C

101972657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45907093-G-A

101973051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45907632-T-A

101973544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45908074-G-A

101973623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45908158-C-T

101973658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45908185-A-G

101974063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45908632-T-C

101974402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45908975-C-G

101974591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909153-C-T

101974732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909294-G-A

http://identifiers.org/hco/10/GRCh38#101975068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45909847-A-C

101975121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909915-G-A

101975121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909915-G-T

101975128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909922-A-T

101975329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910167-T-A

101975329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910167-T-C

101975329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910167-T-G

101975345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910183-G-C

101975345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910183-G-T

101975351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910189-C-G

http://identifiers.org/hco/10/GRCh38#101975363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45910200-C-A

101981221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913770-G-A

101981404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913968-G-T

101984529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914957-A-G

101984588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915020-T-C

101984632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915031-A-G

101984733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915135-G-C

101985889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915182-G-A

http://identifiers.org/hco/10/GRCh38#101985892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45915186-C-A

101986317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915526-G-A

101986340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915548-T-A

101986405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915613-G-A

101986433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915644-C-T

101986554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915757-A-G

101986721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915918-T-A

101986845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916043-T-G

101986849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916046-C-T

101986862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916061-C-T

101986934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916116-T-C

101987105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916277-T-C

101987117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916289-A-G

101987117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916289-A-T

101987158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916314-T-G

101987303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916461-G-A

101987365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916520-T-A

101987381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916530-G-A

101987539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916739-G-A

101989764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920089-C-T

101989986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920309-A-G

101990017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920341-T-C

101990045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920369-T-C

101990173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920481-A-T

http://identifiers.org/hco/10/GRCh38#101990499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45920742-A-C

101990499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920742-A-T

101990660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920899-T-A

101990660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920899-T-C

http://identifiers.org/hco/10/GRCh38#101990718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45920962-C-A

101990718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920962-C-T

http://identifiers.org/hco/10/GRCh38#101990728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45920971-C-A

101990743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920986-T-C

101990867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921356-G-A

101990990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921478-T-C

101991023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921509-G-A

101991813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922102-A-G

101991839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922131-G-T

101991840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922132-G-A

101991840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922132-G-T

http://identifiers.org/hco/10/GRCh38#101991842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45922134-C-A

101991842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922134-C-T

101991845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922137-G-A

101991845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922137-G-T

http://identifiers.org/hco/10/GRCh38#101991884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45922153-C-A

101991884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922153-C-T

101991937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922193-G-T

101991960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922216-C-T

101992103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922360-C-T

101992113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922370-C-T

101992175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922443-G-A

101992175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922443-G-T

101992228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922473-C-T

101992233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922480-G-A

http://identifiers.org/hco/10/GRCh38#101992254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45922501-C-A

101993625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45924884-A-G

101993697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45925860-C-G

101993702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45925865-T-A

101993745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45925906-T-A

101993745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45925906-T-C

101993923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926075-C-T

101994319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926470-T-C

101994618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926745-C-T

101995176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928796-G-A

101995176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928796-G-T

101995259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928844-A-G

101995284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928868-T-G

101995407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928994-C-G

101995418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929003-C-G

101995418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929003-C-T

101995434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929019-A-T

http://identifiers.org/hco/10/GRCh38#101995476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45929358-C-A

101996887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929601-G-T

101996911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929625-T-C

101996919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929633-C-T

http://identifiers.org/hco/10/GRCh38#101997932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45930900-C-A

101998225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45931218-T-C

101998609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45931593-G-A

101998613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45931597-A-G

101998885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45931839-C-T

102001643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45934130-G-A

102001736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934228-A-G

102001805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934297-A-G

102001844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934331-G-A

102001844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934331-G-T

102001922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934411-G-A

102001922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934411-G-C

102001922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45934411-G-T

102001981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45934451-C-G

102002602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45935010-T-G

102004451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45936239-G-A

102006568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45939129-T-C

102006575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45939136-A-G

102009132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940623-C-T

102009226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940697-A-G

102009226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940697-A-T

http://identifiers.org/hco/10/GRCh38#102009293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45940762-C-A

102009293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940762-C-G

102009293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940762-C-T

102009443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45941133-A-G

102009484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941176-A-G

102009485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941177-T-C

102009494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941186-G-A

102009494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941186-G-T

http://identifiers.org/hco/10/GRCh38#102009547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45941220-A-C

102009547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941220-A-G

http://identifiers.org/hco/10/GRCh38#102009579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45941231-C-A

102009579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941231-C-G

102009852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941760-T-A

102009854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941762-A-G

102009869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941777-G-C

102009869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941777-G-T

102009876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941784-T-C

102009937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941844-C-G

102009937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941844-C-T

102010069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941955-A-G

102010081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941967-T-A

102010081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941967-T-C

102010081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941967-T-G

102010117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45941996-T-A

http://identifiers.org/hco/10/GRCh38#102010123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45942002-C-A

102010178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45942039-C-G

102010571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45942424-G-A

102011078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45942926-C-T

102011489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944670-C-G

102011489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944670-C-T

http://identifiers.org/hco/10/GRCh38#102011622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45945020-C-A

102011622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945020-C-T

102011650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945051-G-T

http://identifiers.org/hco/10/GRCh38#102011653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45945054-C-A

102011653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945054-C-T

102011654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945055-G-A

102011654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945055-G-T

102011780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45945176-C-G

102011905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945300-T-C

102012213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945605-T-C

102012276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45945663-G-A

102012665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45946700-C-G

http://identifiers.org/hco/10/GRCh38#102012701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45946730-A-C

102012741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45946768-T-A

102012741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45946768-T-C

http://identifiers.org/hco/10/GRCh38#102012755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45946782-C-A

102012899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45946911-G-T

102013004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947029-A-T

102013118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947184-G-A

102013138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947204-G-A

102013138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947204-G-C

http://identifiers.org/hco/10/GRCh38#102013158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45947222-C-A

102013179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947243-G-T

102013223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947283-A-G

102013252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947313-C-T

102013409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947948-A-G

102013424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45947963-C-T

102013610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948208-T-A

102013610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948208-T-C

102013831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948565-A-G

102013989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45948773-C-T

102013998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45948782-C-G

102013998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45948782-C-T

http://identifiers.org/hco/10/GRCh38#102014045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45948825-C-A

102014045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948825-C-T

102014046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948826-T-C

102014074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948854-G-C

102014166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948933-T-C

102014297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949083-C-T

http://identifiers.org/hco/10/GRCh38#102014316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45949103-C-A

102014953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45949722-C-T

102017248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45952076-G-A

102017444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45952257-C-G

102017453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45952264-C-T

102017668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45952517-C-G

102017925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45952743-C-T

102017985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45952807-G-A

http://identifiers.org/hco/10/GRCh38#102023402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45953537-C-A

102023422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953555-C-T

102023423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953556-G-A

102023423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953556-G-C

102023423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953556-G-T

http://identifiers.org/hco/10/GRCh38#102023440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45953575-A-C

102023441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953576-G-A

102023513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45953639-G-A

102023516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45953642-G-A

102023645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953767-C-T

102023690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45953816-A-G

102023723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45953849-A-G

102023732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45953858-G-C

102023732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45953858-G-T

http://identifiers.org/hco/10/GRCh38#102023747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45953873-C-A

102023797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953923-T-C

102023801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953927-T-A

http://identifiers.org/hco/10/GRCh38#102023828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45953953-A-C

102023831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45953956-G-T

102023941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954040-T-A

102024680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954296-A-T

102024826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954430-A-T

102024944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954471-C-T

http://identifiers.org/hco/10/GRCh38#102025026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45954561-C-A

102025026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954561-C-G

102025026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954561-C-T

102025089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954612-G-C

102025089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954612-G-T

102025130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954652-A-G

102025183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45954708-A-G

102025255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45954780-A-G

http://identifiers.org/hco/10/GRCh38#102025282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45954807-C-A

102025282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954807-C-T

http://identifiers.org/hco/10/GRCh38#102025294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45954819-C-A

102025294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954819-C-T

102025477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45954949-G-T

http://identifiers.org/hco/10/GRCh38#102026066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45955225-C-A

102026066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45955225-C-G

102026066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45955225-C-T

102026179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45955329-G-A

102026190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45955339-G-A

102026190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45955339-G-T

102029577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45961206-G-A

102029613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45961243-G-A

102029631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45961255-G-A

102029710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45961334-C-G

102029710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45961334-C-T

102029797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45961437-T-C

102029797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45961437-T-G

102029826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45961458-C-G

102029826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45961458-C-T

http://identifiers.org/hco/10/GRCh38#102029832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45961464-A-C

102029886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45961522-T-A

102029886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45961522-T-C

102032909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963287-G-A

102032909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963287-G-T

http://identifiers.org/hco/10/GRCh38#102032928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45963302-C-A

http://identifiers.org/hco/10/GRCh38#102032943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45963317-C-A

102032943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45963317-C-T

102032958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45963341-T-G

102033035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45963415-A-T

102033216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963595-G-A

102033228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963607-T-C

102033298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45963673-C-T

http://identifiers.org/hco/10/GRCh38#102033389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45963763-C-A

102033389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45963763-C-T

102033391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45963765-T-A

102033440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963808-G-A

102033440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963808-G-C

102033440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963808-G-T

102033443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963811-G-A

102033443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963811-G-C

102033443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45963811-G-T

http://identifiers.org/hco/10/GRCh38#102040007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45967033-C-A

102040007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45967033-C-T

102040175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45967197-A-G

102040194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45967216-G-T

102040256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45967265-T-C

http://identifiers.org/hco/10/GRCh38#102040292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45967305-C-A

102041372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45968781-T-A

102041372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45968781-T-C

102041616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45969024-G-C

102047504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974201-A-T

102047555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974242-C-T

102047556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974243-G-A

102047821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974497-G-A

102047874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974537-G-A

102047933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974600-G-A

102048022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45974692-G-A

102049112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45975701-T-A

102049112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45975701-T-C

102049187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45975774-T-A

102052919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45980909-C-T

http://identifiers.org/hco/10/GRCh38#102053265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45983848-A-C

102053265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45983848-A-G

102053287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45983870-C-G

http://identifiers.org/hco/10/GRCh38#102053443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45983973-C-A

102053539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45983993-T-C

102054072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45985149-T-C

102055433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986328-G-A

102055603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986452-G-A

102055737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986536-G-A

102055737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986536-G-C

102055752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45986552-A-G

102055809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986613-G-C

102055877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986666-T-C

102055910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986691-G-A

http://identifiers.org/hco/10/GRCh38#102055945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45986723-C-A

http://identifiers.org/hco/10/GRCh38#102055949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45986727-C-A

102055949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45986727-C-T

102055972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45986747-G-A

102055972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45986747-G-T

102055992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25788
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45986767-C-T