http://identifiers.org/hco/2/GRCh38#55634158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29112513-C-A

55634175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3 prime UTR variant
orthologous variants: 29112508-A-G

55634264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3 prime UTR variant
orthologous variants: 29112416-T-G

55635745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111903-A-G

http://identifiers.org/hco/2/GRCh38#55635801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29111847-C-A

55635801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111847-C-T

55635863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111808-G-A

55635916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111762-A-G

55635979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111706-G-A

55635979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111706-G-T

55635985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111700-T-G

55636007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111678-T-C

55636008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111677-T-G

http://identifiers.org/hco/2/GRCh38#55636164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29111534-C-A

55636164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111534-C-T

55636189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 29111510-A-G

55636262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 29111456-G-T

55636311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29111407-C-G

55636311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29111407-C-T

55636315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29111403-G-A

55636315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29111403-G-C

55636315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 29111403-G-T

55636504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29111234-G-A

55636504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29111234-G-T

55636623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110971-C-T

55636656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110944-G-A

55637047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110668-T-C

55637201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110533-C-G

55637547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110208-A-G

55637648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110118-T-C

55637670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29110096-T-C

55640750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29109290-T-A

55640750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29109290-T-C

http://identifiers.org/hco/2/GRCh38#55640755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29109285-A-C

http://identifiers.org/hco/2/GRCh38#55640791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29109253-A-C

55643267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29106972-A-T

55643268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29106971-G-A

55643816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29106703-T-A

55643816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29106703-T-C

55643853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29106666-C-T

55643944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29106579-A-G

55644577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29105853-T-C

http://identifiers.org/hco/2/GRCh38#55644765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29105670-C-A

55644765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105670-C-G

55644765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105670-C-T

55644769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105666-A-G

55644836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105582-T-A

55644836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105582-T-C

55644870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105546-A-G

http://identifiers.org/hco/2/GRCh38#55644871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29105545-C-A

55644926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29105484-A-G

http://identifiers.org/hco/2/GRCh38#55644959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29105444-A-C

55645512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29104742-T-C

55645528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29104728-T-C

55646174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29104443-T-A

55646329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29104293-T-C

55646400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29104228-G-A

http://identifiers.org/hco/2/GRCh38#55646594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29104033-A-C

http://identifiers.org/hco/2/GRCh38#55647312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29103371-C-A

55647325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29103358-T-C

55647330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29103353-A-G

http://identifiers.org/hco/2/GRCh38#55649691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29102902-A-C

55652129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29100880-T-G

55652186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29100822-T-C

55652321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29100710-C-T

http://identifiers.org/hco/2/GRCh38#55652713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29100144-A-C

55653173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29099754-A-G

55653240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29099701-T-C

55653392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29099522-A-G

55653529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29099293-T-C

55653730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29099132-G-A

55653730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29099132-G-C

55654358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29098729-T-C

55654401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29098675-A-T

http://identifiers.org/hco/2/GRCh38#55654975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29098236-C-A

55655037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29098185-T-C

55655872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097754-T-C

http://identifiers.org/hco/2/GRCh38#55656053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29097609-A-C

55656053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097609-A-T

55656225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29097437-A-G

http://identifiers.org/hco/2/GRCh38#55656235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29097427-A-C

55656259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097405-A-G

http://identifiers.org/hco/2/GRCh38#55656343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29097324-C-A

55656376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29097291-A-T

55656422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097217-G-A

55656422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097217-G-T

55656478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097162-T-C

http://identifiers.org/hco/2/GRCh38#55656492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29097148-A-C

55656507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29097117-T-A

55656604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29096988-G-A

55660267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29096732-G-A

55660267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29096732-G-T

55660295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29096703-G-A

55661538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29096008-G-A

55661568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095992-C-T

55661683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095882-G-C

55661811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095759-T-C

55661811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095759-T-G

55661861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095577-A-G

http://identifiers.org/hco/2/GRCh38#55661869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29095569-A-C

55661869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095569-A-G

55661869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095569-A-T

55661874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095564-T-A

http://identifiers.org/hco/2/GRCh38#55661919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29095524-C-A

http://identifiers.org/hco/2/GRCh38#55661920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29095523-A-C

55661920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095523-A-G

55661920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29095523-A-T

http://identifiers.org/hco/2/GRCh38#55662050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29095397-A-C

55664616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29094230-T-C

55664637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29094196-G-A

55664678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29094154-C-T

55664917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29093916-T-C

55665074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29093780-T-A

http://identifiers.org/hco/2/GRCh38#55665788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29093086-C-A

55666023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29092875-G-C

55666126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29092774-T-C

55666211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29092700-A-T

55666563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29092268-A-G

55666643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29092198-C-G

55666852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091918-A-G

55666916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091810-T-A

55667043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29091712-T-A

55667082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29091673-C-T

55667124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091643-G-T

http://identifiers.org/hco/2/GRCh38#55667146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091620-C-A

55667146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091620-C-T

http://identifiers.org/hco/2/GRCh38#55667165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091601-C-A

http://identifiers.org/hco/2/GRCh38#55667229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091537-C-A

55667674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091488-C-G

55667688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091474-A-G

55667689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091473-T-C

http://identifiers.org/hco/2/GRCh38#55667695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091467-C-A

http://identifiers.org/hco/2/GRCh38#55667725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091438-C-A

55667725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091438-C-G

55667729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091434-T-A

55667767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091402-A-G

55667769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091400-A-G

55667802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091369-T-G

http://identifiers.org/hco/2/GRCh38#55667835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091345-A-C

55668019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091164-T-A

http://identifiers.org/hco/2/GRCh38#55668026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29091157-C-A

55668026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091157-C-G

55668026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29091157-C-T

55669721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090943-G-A

55669765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090901-T-C

55670545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090756-C-G

55670614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090696-C-T

55671245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090082-G-A

55671245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090082-G-C

55671245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090082-G-T

55671246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090081-A-T

http://identifiers.org/hco/2/GRCh38#55671269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29090056-A-C

55671269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29090056-A-G

http://identifiers.org/hco/2/GRCh38#55671471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29089862-C-A

55671471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089862-C-T

55671906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089343-G-A

55671906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089343-G-C

55671906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089343-G-T

55671919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089331-T-C

http://identifiers.org/hco/2/GRCh38#55671955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29089301-C-A

55672020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29089248-A-G

55672020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29089248-A-T

55672078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089191-T-A

55672078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089191-T-C

55672121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089152-G-A

55672121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29089152-G-T

http://identifiers.org/hco/2/GRCh38#55672233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29089061-A-C

55672564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088896-T-G

http://identifiers.org/hco/2/GRCh38#55672986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29088509-C-A

55672986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29088509-C-T

http://identifiers.org/hco/2/GRCh38#55673103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29088394-A-C

55673103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088394-A-G

55673127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088370-A-T

55673131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088366-A-G

55679816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088133-G-A

55679816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088133-G-T

55679840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29088113-A-G

55680263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29087714-T-G

55680507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29087450-T-C

http://identifiers.org/hco/2/GRCh38#55680616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29087368-A-C

55680661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29087339-A-G

55680661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29087339-A-T

http://identifiers.org/hco/2/GRCh38#55680926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29087084-A-C

55680926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29087084-A-G

55681032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086956-T-A

55681032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086956-T-C

55681043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086945-G-A

55681043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086945-G-T

55681068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086920-G-A

55682984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086610-T-G

55683078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086556-G-A

55683110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086521-G-C

55683636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085694-T-A

55683636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085694-T-C

55683870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085477-G-A

55683870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085477-G-T

55683979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085381-T-C

55684832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084780-G-A

55684832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084780-G-T

55684837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084775-T-C

55684936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29084710-A-G

http://identifiers.org/hco/2/GRCh38#55684967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#29084679-C-A

55685052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29084594-A-G

55685052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29084594-A-T

55685080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084563-T-C

http://identifiers.org/hco/2/GRCh38#55685095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29084547-C-A

55685109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084523-T-C

55685185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084440-G-A

55685185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084440-G-C

55685185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084440-G-T

55686089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084168-C-T

55686183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084089-G-T

55686237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084046-A-G

55686262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084021-G-C

55686262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084021-G-T

55686264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084019-T-A

55686264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084019-T-C

55686264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084019-T-G

55686278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084008-T-C

http://identifiers.org/hco/2/GRCh38#55686283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29084003-C-A

55686283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084003-C-T

55686297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083991-T-C

55686318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083970-C-T

55686321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083967-C-T

55686323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083965-C-T

http://identifiers.org/hco/2/GRCh38#55686330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29083963-C-A

55686330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083963-C-G

55686344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083948-G-T

http://identifiers.org/hco/2/GRCh38#55686354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29083938-A-C

55686358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083934-G-A

55686358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083934-G-C

55686358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083934-G-T

55686392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29083902-G-A

55686410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29083884-C-T

55686416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29083878-G-A

55686416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29083878-G-C

55686416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29083878-G-T

55686437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29083857-T-C

55686451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29083831-C-G

55686649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083451-T-C

55686783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083318-C-T

55686855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083227-C-G

55687502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083022-T-A

55687502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083022-T-C

http://identifiers.org/hco/2/GRCh38#55687518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29083002-C-A

55687518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083002-C-G

55687518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083002-C-T

55687589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082934-A-G

55687589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082934-A-T

http://identifiers.org/hco/2/GRCh38#55687673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29082875-C-A

55687673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29082875-C-G

55687673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29082875-C-T

55687676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29082872-G-A

55687676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 29082872-G-T

http://identifiers.org/hco/2/GRCh38#55687804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29082756-C-A

55687804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082756-C-T

http://identifiers.org/hco/2/GRCh38#55687812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29082748-C-A

55687812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082748-C-T

55687814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082746-C-T

http://identifiers.org/hco/2/GRCh38#55687824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29082736-C-A

55687824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082736-C-T

55687834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082726-G-A

55687834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082726-G-C

55687878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082682-G-A

55687941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082622-G-A

55687959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082611-T-G

55688425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29082509-C-G

55693540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29081040-T-C

55693540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29081040-T-G

http://identifiers.org/hco/2/GRCh38#55693548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29081032-A-C

55693596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29080989-T-A

55693596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29080989-T-C

55693596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29080989-T-G

http://identifiers.org/hco/2/GRCh38#55693604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#29080977-C-A

55693604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29080977-C-T

55693623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29080958-A-G

55693663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 29080916-C-G

55693663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 29080916-C-T

55693710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 29080869-T-C

55693759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29080820-A-T

55693800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 29080779-G-A

55693800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23166
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 29080779-G-C