197569964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55206198-A-T

197570361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55207401-A-G

197570472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55207498-T-C

http://identifiers.org/hco/2/GRCh38#197570504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55207529-A-C

http://identifiers.org/hco/2/GRCh38#197570534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55207554-C-A

197570570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55207578-T-C

197570582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55207593-C-T

197570837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55209379-A-G

197570936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55209460-C-T

197571008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55209535-G-A

197571092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55209604-T-C

197571209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55209711-G-A

http://identifiers.org/hco/2/GRCh38#197571388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55210362-C-A

197571388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55210362-C-G

http://identifiers.org/hco/2/GRCh38#197571447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55210431-C-A

197571522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55210503-T-C

197571585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55210555-A-G

197571623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55210592-T-A

197571836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55210801-T-G

197571852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55210817-G-T

197571987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55210948-T-C

197571987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 55210948-T-G

197572061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 55211022-C-T

197572083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55211044-A-G

197572248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55211209-G-C

197587874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213544-G-A

http://identifiers.org/hco/2/GRCh38#197587889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55213559-C-A

197587905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213574-C-T

197588016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55213663-C-G

197588016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 55213663-C-T

197588058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213703-G-T

197588100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213788-C-T

http://identifiers.org/hco/2/GRCh38#197588149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55213836-C-A

197588149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55213836-C-T

197595240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223224-T-G

197595251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223235-G-A

197595251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223235-G-T

197595386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223364-C-T

197595431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223408-T-C

197595526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223498-C-T

197595616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223551-T-C

197595689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223646-T-C

197595932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224042-G-A

197595932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224042-G-T

197595933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224043-T-G

197595935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224045-T-C

197595935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224045-T-G

197595972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224082-A-G

197595973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224083-A-G

197595974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224084-G-A

197595974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224084-G-T

197596024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55224142-T-C

197596024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55224142-T-G

197596087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224205-A-G

197596306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225401-G-T

197596397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225504-C-T

197596618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225724-T-A

197596648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225775-A-G

197596673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225800-G-C

197596673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55225800-G-T

197596996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226142-G-C

http://identifiers.org/hco/2/GRCh38#197597032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55226178-C-A

197597085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226229-A-G

197597099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226243-G-A

197597099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226243-G-C

197597214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226363-T-C

197597363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226500-G-A

197597363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226500-G-C

http://identifiers.org/hco/2/GRCh38#197598419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55227046-C-A

197601560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227223-C-G

197601815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227436-T-C

http://identifiers.org/hco/2/GRCh38#197601838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55227453-C-A

http://identifiers.org/hco/2/GRCh38#197612495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55230220-C-A

197612495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230220-C-G

http://identifiers.org/hco/2/GRCh38#197612523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55230251-A-C

197612533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230261-G-A

197612610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230340-A-G

197612881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230611-A-G

197612885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230613-T-A

197612885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230613-T-C

197612977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230677-C-T

197612978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230678-G-A

197613027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230723-G-A

197613141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230820-A-G

197613224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230903-C-T

197613271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230951-T-A

197613271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230951-T-C

197613300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230970-G-A

197613316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55230985-A-G

197613373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231031-C-T

197613708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55231332-C-T

197613889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55231473-A-T

197613902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55231486-C-T

197613929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55231519-C-T

197613933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55231523-A-G

197613984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231571-T-C

197614236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55231819-T-C

197615746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233296-A-G

197615778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233318-T-C

197615778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233318-T-G

197615779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233319-G-A

197615779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233319-G-C

197615779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233319-G-T

197615866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233393-T-C

http://identifiers.org/hco/2/GRCh38#197615938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55233465-A-C

197615938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55233465-A-G

197615956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55233483-A-G

197615956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 55233483-A-T

197615985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55233512-T-C

197615994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233521-A-G

http://identifiers.org/hco/2/GRCh38#197616040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55233567-C-A

197616040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55233567-C-T

197616965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234118-G-A

197617011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234163-C-T

197617024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234176-G-A

197617028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234180-T-C

http://identifiers.org/hco/2/GRCh38#197617189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55234353-A-C

197617243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234425-C-G

197617263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234452-A-G

197617575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55234617-G-C

197617809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55234684-A-G

197617809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55234684-A-T

197617862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55234737-C-T

197617937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55234811-T-C

197617955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55234828-T-C

http://identifiers.org/hco/2/GRCh38#197619794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55235341-C-A

197619863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55235393-C-T

197620088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55235579-T-A

197620418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55236139-T-G

197620438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55236158-A-G

197620571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55236609-G-T

197627163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55240001-G-A

197627419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55240440-A-G

197627740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55240636-T-C

http://identifiers.org/hco/2/GRCh38#197627803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55240698-A-C

197627835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55240735-A-T

http://identifiers.org/hco/2/GRCh38#197628117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55240991-C-A

197630554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55242090-G-A

197630687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55242177-C-T

197630754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55242244-C-T

http://identifiers.org/hco/2/GRCh38#197630970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55243300-C-A

197630970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55243300-C-T

197630988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55243319-A-G

http://identifiers.org/hco/2/GRCh38#197630994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55243325-A-C

197630994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55243325-A-G

197631027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense variant
orthologous variants: 55243358-G-T

197631222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: undefined
orthologous variants: 55243553-T-C

197631226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55243557-C-T

197633176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245064-A-G

197633542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245328-C-G

http://identifiers.org/hco/2/GRCh38#197633582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55245366-C-A

197633582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245366-C-G

197633582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245366-C-T

http://identifiers.org/hco/2/GRCh38#197633842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55245619-A-C

197633870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense variant
orthologous variants: 55245647-C-G

197633871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense variant
orthologous variants: 55245648-C-T

197633888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense variant
orthologous variants: 55245665-A-G

197634026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245801-A-G

197634069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245836-T-A

197634120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55245883-A-T

197634248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55246182-T-C

197634290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55246226-G-C

197634491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55246421-G-C

197634519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55246449-A-G

197634519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55246449-A-T

197634553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55246481-T-C

197641924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55248138-C-T

197642178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55248396-A-G

197642218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55248435-C-T

197644187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: missense variant
orthologous variants: 55250338-T-C

197644227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: synonymous variant
orthologous variants: 55250378-G-A

197644363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55250502-C-G

197644375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55250514-A-T

197644456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55250585-A-G

197644625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55250706-C-T

197644956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/2/GRCh38#197646702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55253498-C-A

197646736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55253532-G-A

197646736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55253532-G-T

197646756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55253552-G-T

197647058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55253743-A-G

197647459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55253999-C-T

197648268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55254846-C-G

197648268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55254846-C-T

197648801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55255403-A-G

197657971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55256331-G-C

197658643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55256522-A-G

http://identifiers.org/hco/2/GRCh38#197658821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55256680-A-C

197658821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55256680-A-G

197658821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55256680-A-T

197658967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55256818-T-A

197659147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55257157-A-G

197659147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55257157-A-T

197669375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55258333-C-T

197669394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55258345-T-G

197669452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55258392-C-T

197669478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55258418-G-A

197673301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55263342-A-G

197673359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55263404-T-A

197673382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55263424-G-A

197673597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55263644-C-G

197673743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55263781-G-A

197673817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55263851-T-G

http://identifiers.org/hco/2/GRCh38#197674055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55264071-A-C

197674131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55264137-G-T

197674212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55264226-A-G

http://identifiers.org/hco/2/GRCh38#197674593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55264548-C-A

197674593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55264548-C-T

http://identifiers.org/hco/2/GRCh38#197674623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55264587-A-C

197674670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55264636-C-T

197675102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265053-C-T

197675122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265073-A-G

197675175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265135-G-T

197675232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265192-G-T

197675246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265205-T-A

197675274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265232-T-A

http://identifiers.org/hco/2/GRCh38#197675297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265257-A-C

http://identifiers.org/hco/2/GRCh38#197675310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265270-C-A

197675310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265270-C-T

197675342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: synonymous variant
orthologous variants: 55265302-T-C

197675444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: synonymous variant
orthologous variants: 55265404-A-G

197675483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55265444-T-C

197675510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55265477-A-G

197675518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55265485-G-C

197675518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55265485-G-T

197675545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55265512-A-G

http://identifiers.org/hco/2/GRCh38#197675576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265542-A-C

197675579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55265545-A-T

http://identifiers.org/hco/2/GRCh38#197675591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265557-A-C

197675648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265570-G-C

197675648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265570-G-T

197675660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265582-G-A

197675660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265582-G-T

http://identifiers.org/hco/2/GRCh38#197675703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265622-A-C

197675727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265646-A-G

http://identifiers.org/hco/2/GRCh38#197675758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265677-C-A

197675758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: intron variant
orthologous variants: 55265677-C-T

197675843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5 prime UTR variant
orthologous variants: 55265766-A-G

http://identifiers.org/hco/2/GRCh38#197676039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265937-C-A

http://identifiers.org/hco/2/GRCh38#197676040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26402
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#55265938-A-C