55675954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5083936-C-T

55676675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084543-T-A

55676675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084543-T-G

55676711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084579-T-G

55676746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084610-A-G

55676826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084714-T-C

55676826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084714-T-G

http://identifiers.org/hco/19/GRCh38#55676886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5084786-C-A

55676886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084786-C-T

55677034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5084936-A-G

55677181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant
orthologous variants: 5085083-C-G

55677517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085551-T-G

55677667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant
orthologous variants: 5085677-G-C

http://identifiers.org/hco/19/GRCh38#55677719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085732-C-A

55677719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant
orthologous variants: 5085732-C-G

http://identifiers.org/hco/19/GRCh38#55677769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085791-C-A

55677769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085791-C-G

55677769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085791-C-T

55677793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085841-G-T

55677797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085845-T-G

55677801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085849-T-C

55677805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085853-G-A

55677805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085853-G-T

55677818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085866-G-A

55677818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085866-G-T

http://identifiers.org/hco/19/GRCh38#55677822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085870-C-A

55677822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085870-C-G

55677822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085870-C-T

55677824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085882-T-C

http://identifiers.org/hco/19/GRCh38#55677828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085886-C-A

55677828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085886-C-T

55677832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085890-T-C

55677832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085890-T-G

http://identifiers.org/hco/19/GRCh38#55677848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085906-C-A

55677848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085906-C-T

http://identifiers.org/hco/19/GRCh38#55677852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085910-C-A

55677852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085910-C-T

http://identifiers.org/hco/19/GRCh38#55677856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5085914-C-A

55677856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085914-C-G

55677856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5085914-C-T

55678483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5086622-G-A

55678483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5086622-G-T

http://identifiers.org/hco/19/GRCh38#55678519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5086654-C-A

55678519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 5086654-C-T

http://identifiers.org/hco/19/GRCh38#55678573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5086708-C-A

55678615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 5086741-G-A

http://identifiers.org/hco/19/GRCh38#55678702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5086828-A-C

55678869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5086995-T-C

55678869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5086995-T-G

55678901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5087011-G-A

http://identifiers.org/hco/19/GRCh38#55678925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5087036-C-A

55678925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5087036-C-T

55678964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5087058-T-A

55679509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088584-C-T

55679515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088588-G-A

55679515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088588-G-C

http://identifiers.org/hco/19/GRCh38#55679525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5088594-C-A

55679525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088594-C-T

55679682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088723-A-T

55679732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088760-G-C

55679783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088797-A-G

55679857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5088873-G-T

55679904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5089390-C-G

55679904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5089390-C-T

55679968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5089467-G-A

55679968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5089467-G-T

55679984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5089479-C-T

55683700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5091013-G-A

55683700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5091013-G-C

55683762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5091075-A-G

55683882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5091191-C-G

55683938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5091247-A-G

55684501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092170-G-T

55684785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092362-C-T

http://identifiers.org/hco/19/GRCh38#55684840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5092416-C-A

55684840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092416-C-T

55684854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092430-G-T

55684859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092435-G-C

55684872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092445-G-A

55684890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092463-T-G

55685219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092761-T-C

55685287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092817-G-A

http://identifiers.org/hco/19/GRCh38#55685325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5092859-C-A

55685325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092859-C-T

55685337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5092868-A-G

55688106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095161-G-T

55688111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095166-G-A

55688130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095204-G-A

55688140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095214-G-C

55688234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095296-G-A

55688462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095527-A-G

55688632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095643-C-G

55688768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5095759-G-C

http://identifiers.org/hco/19/GRCh38#55688904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5095874-C-A

55688904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5095874-C-G

55688904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5095874-C-T

55688910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5095880-G-A

55688910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5095880-G-T

http://identifiers.org/hco/19/GRCh38#55689098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096060-C-A

http://identifiers.org/hco/19/GRCh38#55689184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096173-C-A

55689184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096173-C-T

55689193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096182-G-A

55689193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096182-G-T

http://identifiers.org/hco/19/GRCh38#55689204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096193-C-A

55689204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096193-C-G

55689204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096193-C-T

http://identifiers.org/hco/19/GRCh38#55689301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096315-C-A

55689301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5096315-C-T

http://identifiers.org/hco/19/GRCh38#55689403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096408-C-A

55689403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096408-C-T

55689417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096422-A-G

http://identifiers.org/hco/19/GRCh38#55689427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096432-C-A

55689427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096432-C-G

55689427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096432-C-T

http://identifiers.org/hco/19/GRCh38#55689477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096455-A-C

55689477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096455-A-G

http://identifiers.org/hco/19/GRCh38#55689486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096464-C-A

55689486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096464-C-T

http://identifiers.org/hco/19/GRCh38#55689502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096473-A-C

55689502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096473-A-G

55689502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096473-A-T

55689511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096482-A-G

55689522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096496-G-A

55689607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096593-C-T

55689725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096742-T-G

55689740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096757-G-A

55689740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096757-G-T

55689757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096775-T-C

55689798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096825-C-G

55689798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5096825-C-T

http://identifiers.org/hco/19/GRCh38#55689884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5096915-C-A

55689884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5096915-C-T

55689902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5096933-G-A

55689947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense variant
orthologous variants: 5096978-G-C

55689947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense variant
orthologous variants: 5096978-G-T

http://identifiers.org/hco/19/GRCh38#55691043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5097408-A-C

55691085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097448-G-A

55691085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097448-G-C

55691209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097530-G-T

55691298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097615-G-A

http://identifiers.org/hco/19/GRCh38#55691333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5097652-C-A

55691333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097652-C-G

55691355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097672-G-A

55691360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097677-G-A

55691360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097677-G-T

55691377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097692-C-T

55691503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097785-T-G

55691589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097877-G-A

55691629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097887-T-C

55691638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097896-G-A

55691638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5097896-G-T

55691780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: synonymous variant
orthologous variants: 5097979-C-T

55691825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: synonymous variant
orthologous variants: 5098024-C-G

55691825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: synonymous variant
orthologous variants: 5098024-C-T

55691848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense variant
orthologous variants: 5098047-T-G

http://identifiers.org/hco/19/GRCh38#55691873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5098072-C-A

55691873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: synonymous variant
orthologous variants: 5098072-C-T

http://identifiers.org/hco/19/GRCh38#55691902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5098101-C-A

55692117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098297-A-G

55692172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098320-G-A

55692172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098320-G-T

55692181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098325-G-A

55692181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098325-G-T

55692478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098482-C-T

55692618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5098587-A-G

http://identifiers.org/hco/19/GRCh38#55692654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5098610-C-A

55692654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5098610-C-G

55692654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5098610-C-T

55692733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5098689-G-A

55692733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5098689-G-T

http://identifiers.org/hco/19/GRCh38#55692777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5098733-C-A

55692777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5098733-C-T

55693036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 5098972-A-G

55693091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5098999-T-G

http://identifiers.org/hco/19/GRCh38#55693140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5099055-C-A

55693140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5099055-C-G

55693165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5099080-T-C

55693172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5099086-G-C

55693172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5099086-G-T

http://identifiers.org/hco/19/GRCh38#55693190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5099104-C-A

55693190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5099104-C-T

55694600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100019-T-C

55694627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100049-G-A

55694627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100049-G-C

55694627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100049-G-T

55694636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100058-G-T

http://identifiers.org/hco/19/GRCh38#55694642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5100072-C-A

http://identifiers.org/hco/19/GRCh38#55694666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5100096-C-A

55694666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100096-C-T

55694986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100413-G-A

55694986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100413-G-T

http://identifiers.org/hco/19/GRCh38#55695013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5100446-C-A

55695013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100446-C-T

http://identifiers.org/hco/19/GRCh38#55695030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5100462-C-A

55695066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100498-C-T

55695079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron variant
orthologous variants: 5100513-A-G

55695269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 5100692-C-T

55695299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 5100722-G-A

55695299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 5100722-G-C

55695299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 5100722-G-T

http://identifiers.org/hco/19/GRCh38#55695335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5100758-C-A

55695577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5101004-T-A

55695577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5101004-T-C

55695577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5101004-T-G

http://identifiers.org/hco/19/GRCh38#55695799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5101217-C-A

55695799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 5101217-C-T

55695916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101326-A-G

55695916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101326-A-T

55695929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101339-T-G

55696022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101350-G-A

http://identifiers.org/hco/19/GRCh38#55696072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5101368-A-C

55696072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101368-A-G

55696162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101404-A-G

http://identifiers.org/hco/19/GRCh38#55696199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5101440-C-A

55696199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101440-C-T

55696216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101457-G-A

55696216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101457-G-T

http://identifiers.org/hco/19/GRCh38#55696224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5101465-C-A

http://identifiers.org/hco/19/GRCh38#55696248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5101478-C-A

55696252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101482-G-T

55696277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101503-G-T

55696278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101504-T-C

55696284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101510-G-A

55696284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101510-G-T

55696287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5101513-G-A

55696317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101541-A-G

55696407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101595-A-G

55696429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101613-T-C

55696443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101627-G-A

http://identifiers.org/hco/19/GRCh38#55696444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5101628-C-A

55696444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101628-C-T

55696482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101663-G-T

55696503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101683-G-A

55696532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101706-T-C

55696567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101729-G-A

55696567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101729-G-T

55696598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101763-T-A

55696598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101763-T-C

55696606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101771-G-A

55696606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101771-G-T

55696646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101802-T-C

55696676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101835-C-T

55696677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101836-A-G

55696677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5101836-A-T

55697669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5102800-C-T

http://identifiers.org/hco/19/GRCh38#55697679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#5102810-C-A

55697679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21604
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5102810-C-G