243124488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176561284-A-T

243124648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176561434-C-T

243125014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176561801-G-A

243125530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176562312-C-T

243125933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176562726-G-A

243125960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176562752-G-C

243126047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176562841-G-A

243126047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 176562841-G-T

243126205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563009-A-T

243126217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563021-G-A

http://identifiers.org/hco/1/GRCh38#243126300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176563103-C-A

243126300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563103-C-G

243126300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563103-C-T

243126343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563144-G-T

243126408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563207-G-C

243126408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563207-G-T

243126444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176563241-G-C

243126904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176563713-A-G

http://identifiers.org/hco/1/GRCh38#243128218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176564337-C-A

243128218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176564337-C-T

243128880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176564675-A-G

http://identifiers.org/hco/1/GRCh38#243128894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176564689-C-A

243128941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176564737-A-T

http://identifiers.org/hco/1/GRCh38#243129301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176565034-C-A

243129301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176565034-C-G

243129301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176565034-C-T

http://identifiers.org/hco/1/GRCh38#243129525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176565239-C-A

243129525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176565239-C-T

http://identifiers.org/hco/1/GRCh38#243129570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176565296-C-A

243129570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176565296-C-T

243129614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176565328-A-G

243129627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176565341-T-C

http://identifiers.org/hco/1/GRCh38#243136103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176566626-A-C

243136187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176566691-A-G

243136202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176566706-G-A

http://identifiers.org/hco/1/GRCh38#243136262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176566759-A-C

243136262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176566759-A-G

243136283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176566775-A-G

243136300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176566792-T-A

243136300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176566792-T-C

http://identifiers.org/hco/1/GRCh38#243136356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176566840-A-C

243136493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176566957-C-T

243136613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176567060-C-T

243136729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176567143-G-T

243140146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176567694-A-G

http://identifiers.org/hco/1/GRCh38#243140169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176567716-C-A

243140169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176567716-C-T

http://identifiers.org/hco/1/GRCh38#243140284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176567821-C-A

243140284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176567821-C-T

http://identifiers.org/hco/1/GRCh38#243140308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176567845-C-A

243140308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176567845-C-T

http://identifiers.org/hco/1/GRCh38#243140323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176567860-C-A

243141498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176569008-T-C

243141731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176569529-G-C

243141825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176569632-T-C

243142195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176569946-T-C

243142355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 176570106-A-G

http://identifiers.org/hco/1/GRCh38#243142578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176570323-C-A

243142578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176570323-C-T

243144117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176571893-A-G

http://identifiers.org/hco/1/GRCh38#243144945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176573405-A-C

243145121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176573556-T-C

http://identifiers.org/hco/1/GRCh38#243154508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176575037-C-A

243154760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176575271-T-C

243155000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176575489-C-G

243155001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176575490-C-G

243155038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176575527-A-G

243155852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176576912-C-T

243155933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176576994-G-A

243156189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176577242-T-C

243156789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 176578046-G-A

243156789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 176578046-G-C

243156789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 176578046-G-T

243157559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176578754-C-T

243157570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176578765-C-T

243160468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176579762-T-G

243160576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176579867-T-C

243160613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176579911-G-A

243160713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176580009-A-G

243160713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176580009-A-T

243161785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176580622-C-T

243162198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176580888-T-A

243162599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176581250-G-A

243163311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 176581965-T-A

243163311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 176581965-T-C

243163452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176582104-A-G

243163564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176582196-T-C

http://identifiers.org/hco/1/GRCh38#243163715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176582334-C-A

243163715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176582334-C-T

243164204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176582663-T-G

243164390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: synonymous variant
orthologous variants: 176582838-T-C

243164399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense variant
orthologous variants: 176582847-A-T

243164435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: synonymous variant
orthologous variants: 176582883-A-G

243164594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: synonymous variant
orthologous variants: 176583042-T-C

243164782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176583233-C-T

http://identifiers.org/hco/1/GRCh38#243164888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176583339-A-C

243164888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176583339-A-G

243164933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176583384-A-G

243164971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176583422-T-C

243165164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176583606-T-C

http://identifiers.org/hco/1/GRCh38#243165188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176583630-A-C

243165188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176583630-A-G

243165188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176583630-A-T

http://identifiers.org/hco/1/GRCh38#243165233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176583678-A-C

243165236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176583681-T-C

243165335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176583780-T-C

243165464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176583909-T-C

243165806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176584245-G-A

http://identifiers.org/hco/1/GRCh38#243165905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176584344-C-A

243165905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176584344-C-T

243166100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 176584533-C-T

243169097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176585539-T-C

243169529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176585869-A-G

243171216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176587651-A-G

243171348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176587772-A-G

243171909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176588422-C-T

http://identifiers.org/hco/1/GRCh38#243172945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176589161-C-A

243172962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176589178-G-A

243172962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176589178-G-T

243174503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176589986-T-G

http://identifiers.org/hco/1/GRCh38#243174867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176590361-C-A

243174867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176590361-C-T

243175157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 176590615-G-T

243175220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176590712-C-G

243175531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176591143-T-C

243176156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176591453-G-A

http://identifiers.org/hco/1/GRCh38#243176236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176591531-C-A

243176440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176591697-G-T

243176466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176591723-C-T

243176568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176591822-T-C

http://identifiers.org/hco/1/GRCh38#243176862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176592118-C-A

243176936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176592189-C-T

243176968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176592219-G-C

243177388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176592696-C-T

243178340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176593486-T-A

243178340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176593486-T-G

243178708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176593918-A-T

243183297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176594644-C-T

243183921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176595213-A-G

243184115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176595410-G-T

243184328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176595602-G-T

243184526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176595767-T-A

243184842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176596053-T-C

243185282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176596396-A-G

http://identifiers.org/hco/1/GRCh38#243185653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176596676-A-C

243185689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176596712-G-T

243186219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 176597239-C-T

http://identifiers.org/hco/1/GRCh38#243186362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176597376-C-A

243186362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 176597376-C-T

243186374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 176597388-G-T

243186609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176597623-A-G

243186609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176597623-A-T

http://identifiers.org/hco/1/GRCh38#243186664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176597680-C-A

243186822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176598043-G-A

243187120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176598374-T-G

243187558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176598944-T-G

243187698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176599068-G-T

243189210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176600448-C-G

243189210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176600448-C-T

243189273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176600514-C-T

243189668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176600783-A-T

243189706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176600829-G-C

243189853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176600964-C-T

243190125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176601181-T-C

243190470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176601474-A-T

243190589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176601597-G-A

243190987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176601975-T-C

243191094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 176602076-T-C

243191440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant
orthologous variants: 176602422-T-G

243191464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant
orthologous variants: 176602446-T-G

243191477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, stop_gained
orthologous variants: 176602459-T-A

http://identifiers.org/hco/1/GRCh38#243191485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176602467-A-C

243191485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant
orthologous variants: 176602467-A-G

243191485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, missense_variant
orthologous variants: 176602467-A-T

http://identifiers.org/hco/1/GRCh38#243191565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176602545-C-A

243192256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603170-T-C

243192276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603190-T-A

243192331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603230-T-C

243192467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603325-C-T

243192476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603334-T-C

http://identifiers.org/hco/1/GRCh38#243192542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176603411-C-A

http://identifiers.org/hco/1/GRCh38#243192571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176603439-A-C

243192585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603452-A-G

243192635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176603498-C-G

243194643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176604876-T-C

243194825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176605065-T-C

243196520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176605651-T-C

243196529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176605658-C-T

243197053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176606111-G-C

243197492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176606523-G-A

243197577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176606608-C-T

243197965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176606944-G-A

243199072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense variant
orthologous variants: 176607839-C-T

243199133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: synonymous variant
orthologous variants: 176607900-A-G

243199133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense variant
orthologous variants: 176607900-A-T

243199323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608074-G-A

243199323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608074-G-C

243199323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608074-G-T

243199358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608089-G-A

243199434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608159-A-G

243199509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608240-T-G

243199730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608452-G-T

243200387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608944-T-C

243200433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176608991-G-T

243200521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense variant
orthologous variants: 176609820-T-C

243200521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: missense variant
orthologous variants: 176609820-T-G

243200792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: synonymous variant
orthologous variants: 176610078-A-G

243200923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176610375-T-C

243200963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176610435-G-A

243200963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176610435-G-C

243200963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176610435-G-T

243200995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176610563-G-A

243201198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176610774-G-A

243203427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176612527-C-T

243203439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176612539-T-C

243203489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176612578-A-G

http://identifiers.org/hco/1/GRCh38#243203502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176612591-C-A

243203502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176612591-C-T

243203550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176612640-T-A

243208863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176613968-A-G

243208863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176613968-A-T

243210387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron variant
orthologous variants: 176614934-G-T

243211374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615645-G-A

243211464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615708-T-C

243211563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615803-A-G

http://identifiers.org/hco/1/GRCh38#243211582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176615822-C-A

243211583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615823-C-G

243211583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615823-C-T

243211706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615906-T-C

http://identifiers.org/hco/1/GRCh38#243211709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176615909-C-A

243211709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615909-C-T

243211710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176615910-T-C

http://identifiers.org/hco/1/GRCh38#243212017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176616148-C-A

243212017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616148-C-T

http://identifiers.org/hco/1/GRCh38#243212038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176616165-C-A

243212038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616165-C-G

243212097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616206-G-A

243212097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616206-G-C

243212097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616206-G-T

243212109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616216-A-G

243212167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616269-C-G

243212167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176616269-C-T

243213129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176616978-G-T

243213387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176617240-G-A

243213664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176617532-T-C

243218645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176618481-G-T

243218884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176618709-T-C

243220863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176619604-C-T

243220865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176619606-G-A

243220933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176619676-A-G

243220969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176619708-T-C

243221821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 176620199-G-C

http://identifiers.org/hco/1/GRCh38#243222205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176620612-A-C

243225105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176621021-G-T

243228508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176623263-A-T

243228982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176623819-T-C

http://identifiers.org/hco/1/GRCh38#243232893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176625146-C-A

243233119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176625418-C-T

243233432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176625892-T-C

243233494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176625994-G-A

243233515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176626022-C-T

243233547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176626069-C-G

http://identifiers.org/hco/1/GRCh38#243233557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176626079-C-A

243233557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176626079-C-G

243233619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176626125-G-C

http://identifiers.org/hco/1/GRCh38#243233728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176626193-A-C

243233728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176626193-A-G

http://identifiers.org/hco/1/GRCh38#243233732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176626197-C-A

243234338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176626660-T-C

243237970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176629442-T-G

243246708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176632870-G-C

243246710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176632872-T-C

243246716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176632877-G-A

243246716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176632877-G-T

243250790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176635891-G-T

243250928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176636039-C-G

243251607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176637710-C-T

243251641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176637744-T-A

243253055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 176639668-C-T

243253322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176639869-G-A

243253545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176640113-T-C

243254092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176640647-G-A

http://identifiers.org/hco/1/GRCh38#243254351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#176640885-C-A

243254430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176640964-A-G

243254454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176640988-C-T

243254510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176641044-G-A

243254510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176641044-G-T

243254919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176641365-C-T

243254930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176641376-G-A

http://identifiers.org/hco/1/GRCh38#243254966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#176641413-C-A

243254966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 176641413-C-T

243255019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 176641449-G-T

http://identifiers.org/hco/1/GRCh38#243255114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#176641533-C-A

243255114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 176641533-C-G

243255114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 176641533-C-T

243255138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 176641557-C-T

http://identifiers.org/hco/1/GRCh38#243255158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#176641568-C-A

243255158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 176641568-C-T

243255181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 176641591-G-A

243255181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 176641591-G-T

http://identifiers.org/hco/1/GRCh38#243255249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#176641659-C-A

243255249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 176641659-C-G

243255249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 176641659-C-T

243255434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5 prime UTR variant
orthologous variants: 176641844-G-C

243255749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28920
most severe consequence: 5 prime UTR variant
orthologous variants: 176642141-C-T