http://identifiers.org/hco/1/GRCh38#74568217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154473380-A-C

74568622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472988-T-A

74568731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472877-G-C

74568731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472877-G-T

http://identifiers.org/hco/1/GRCh38#74568733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154472875-C-A

74568733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472875-C-T

74568810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472811-A-G

74569197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472448-T-A

74569197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472448-T-C

74569319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472341-G-A

74569319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472341-G-T

74569388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472278-T-C

74569495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472174-G-A

74569495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472174-G-T

74569620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154472063-T-G

74569848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154471832-T-A

74570070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154471748-T-C

http://identifiers.org/hco/1/GRCh38#74570142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154471682-C-A

http://identifiers.org/hco/1/GRCh38#74570160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154471662-C-A

74570160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154471662-C-T

74570306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154471516-A-G

74570358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 154471482-G-T

74570477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154471384-A-T

74570497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154471361-A-G

74570507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154471352-G-T

74570616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154471239-C-T

74570649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154471186-A-T

74570700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154471135-C-T

74570846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154470833-A-G

http://identifiers.org/hco/1/GRCh38#74570852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154470827-C-A

74570908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154470766-T-A

74570925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154470749-C-T

http://identifiers.org/hco/1/GRCh38#74570957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154470720-C-A

74570957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154470720-C-T

74570969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154470708-T-C

http://identifiers.org/hco/1/GRCh38#74571150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154470552-A-C

74571156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154470546-G-A

74571175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470527-T-A

74571221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470484-G-A

74571221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470484-G-C

74571221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470484-G-T

74571222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154470483-T-C

http://identifiers.org/hco/1/GRCh38#74571271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154470445-C-A

74571271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470445-C-T

74571299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470417-C-T

74571337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470379-G-C

74571402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154470301-G-A

74571402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154470301-G-C

74571511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470199-G-A

74571511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470199-G-T

http://identifiers.org/hco/1/GRCh38#74571638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#154470081-C-A

74571638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470081-C-T

74571704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154470018-T-C

74571793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469971-G-A

74571810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469954-T-G

74571869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469889-T-C

http://identifiers.org/hco/1/GRCh38#74571881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#154469877-C-A

74571881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469877-C-T

74571885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154469873-A-G

http://identifiers.org/hco/1/GRCh38#74571956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154469790-C-A

74571956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469790-C-G

74571956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469790-C-T

74572021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469731-G-T

74572088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469665-G-A

74572088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469665-G-T

74572339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469449-G-A

http://identifiers.org/hco/1/GRCh38#74572361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154469427-C-A

74572361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469427-C-T

74572362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469426-T-A

74572505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469286-A-T

74572506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154469285-T-C

74572507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469284-G-A

74572507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469284-G-T

74572584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469207-C-G

74572722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154469096-G-A

74572805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154469016-C-T

74572842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154468979-T-C

74572874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468947-C-T

74573092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468729-T-C

74573141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468656-C-G

74573149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468648-C-G

74573149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468648-C-T

http://identifiers.org/hco/1/GRCh38#74573252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#154468551-C-A

http://identifiers.org/hco/1/GRCh38#74573280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154468523-C-A

74573280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154468523-C-T

74573286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 154468517-G-T

http://identifiers.org/hco/1/GRCh38#74573303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154468503-C-A

74573303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468503-C-T

74573306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 154468500-C-T

74573800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467459-T-C

74573910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467384-T-A

74573912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467382-A-G

74573929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467362-T-C

74574535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467129-C-G

74574535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467129-C-T

http://identifiers.org/hco/1/GRCh38#74574606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154467048-C-A

74574606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154467048-C-T

http://identifiers.org/hco/1/GRCh38#74575364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154464483-A-C

http://identifiers.org/hco/1/GRCh38#74575448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154464395-A-C

74575467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154464375-T-A

74575505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154464335-G-A

74575545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154464295-C-T

http://identifiers.org/hco/1/GRCh38#74575749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154464091-C-A

74575749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154464091-C-T

74576013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463841-A-G

74576107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463742-C-T

74576370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463505-T-C

74576412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463480-G-T

74576485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463418-T-C

74576780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463268-T-C

74576780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463268-T-G

74576845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463229-A-G

74576849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463225-T-A

http://identifiers.org/hco/1/GRCh38#74576859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154463216-C-A

74576885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463188-G-A

74576885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463188-G-C

74576886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463187-A-G

http://identifiers.org/hco/1/GRCh38#74576904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154463179-C-A

74576904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154463179-C-T

74577057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463028-G-C

74577057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463028-G-T

74577058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463027-G-A

74577058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154463027-G-T

74577126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154462969-A-G

http://identifiers.org/hco/1/GRCh38#74577136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462959-A-C

74577136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154462959-A-G

74577144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154462951-A-G

74577211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154462886-A-G

http://identifiers.org/hco/1/GRCh38#74577224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462873-C-A

74577224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154462873-C-T

74577326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154462743-T-A

http://identifiers.org/hco/1/GRCh38#74577328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462741-C-A

http://identifiers.org/hco/1/GRCh38#74577402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462667-C-A

74577402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154462667-C-G

74577459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154462613-G-A

http://identifiers.org/hco/1/GRCh38#74577853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462222-C-A

http://identifiers.org/hco/1/GRCh38#74577995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154462079-A-C

74577995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154462079-A-G

74578161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154461965-T-C

74578256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154461870-A-G

74578376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154461760-C-T

74578440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154461699-C-G

http://identifiers.org/hco/1/GRCh38#74578455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154461684-C-A

74578465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154461675-C-T

http://identifiers.org/hco/1/GRCh38#74578598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154461593-C-A

74578625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154461566-T-G

http://identifiers.org/hco/1/GRCh38#74578635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154461556-C-A

74578635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154461556-C-T

74578791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461478-T-G

74579051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461223-C-T

74579181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461090-A-G

74579181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154461090-A-T

74579370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

74579415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -A-G

74579456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -A-T

74582271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460208-A-T

74582352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460124-T-C

74582352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460124-T-G

74582396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460078-C-T

74582438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154460047-A-T

74583872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459907-T-A

74583994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459786-A-G

74584057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459722-T-C

74584091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459690-C-T

74584262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459537-A-G

74584420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459348-G-A

74584527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459256-T-C

74584564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459122-T-C

74584637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154459053-C-G

http://identifiers.org/hco/1/GRCh38#74584804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154458923-C-A

http://identifiers.org/hco/1/GRCh38#74584894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154458836-A-C

74584908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458831-T-C

74584961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458778-A-G

74586380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458551-C-T

74586570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458369-A-G

74586570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458369-A-T

74586577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458362-G-A

74586596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458347-T-C

74586596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458347-T-G

74586756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458161-G-A

74586757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458160-A-G

74586800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458121-G-T

74586831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458101-T-C

74586870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154458065-T-C

74587384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457877-T-A

74587487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457783-A-G

74587522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457749-G-T

74587523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154457748-A-G

74588149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154455713-C-G

74588374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154455508-A-G

74588560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154455355-C-T

74589179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454788-T-C

74589239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454734-A-G

74589246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454727-C-T

74589255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154454718-T-C

74589423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154454553-T-C

74589423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154454553-T-G

74589545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154454439-T-C

74589585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154454407-T-C

74589743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 154454282-G-A

74589743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 154454282-G-C

74589811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154454214-C-T

74589873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154454158-T-G

74590159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453872-A-T

74590819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453587-A-G

74590909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453505-T-C

74590909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453505-T-G

74591059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453377-T-C

74591452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154453021-G-A

74591799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154452672-T-C

74591939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154452532-T-A

http://identifiers.org/hco/1/GRCh38#74591989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154452469-C-A

http://identifiers.org/hco/1/GRCh38#74592108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154452353-C-A

74592108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 154452353-C-T

http://identifiers.org/hco/1/GRCh38#74592204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154452285-C-A

74592573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451970-A-G

74592716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451832-T-A

74592968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451555-C-T

74593026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451504-A-G

74593038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451494-T-G

74593056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451484-G-C

74593130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451418-C-G

74593173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451376-A-G

74593174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451375-T-C

http://identifiers.org/hco/1/GRCh38#74594523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154451250-A-C

74594551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154451222-C-T

74594984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450860-A-G

74594984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450860-A-T

74594993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450851-G-T

74595230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450622-A-T

74595272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154450584-T-C

74596756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448870-G-T

74596823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448805-G-A

http://identifiers.org/hco/1/GRCh38#74596903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154448743-C-A

74596903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448743-C-T

74596904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448742-G-A

74596904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448742-G-T

74596988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448659-G-A

74597570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448116-T-C

74597632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154448051-A-T

74599760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154444893-G-T

http://identifiers.org/hco/1/GRCh38#74599770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154444892-C-A

74599770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154444892-C-T

74600606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154444067-T-G

74600909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443769-G-A

74600909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443769-G-C

74600909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443769-G-T

74600911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443767-G-T

74600928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443750-A-G

74600986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154443700-T-C

74601702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154441387-G-A

74602003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154441102-G-A

74602191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440949-A-T

http://identifiers.org/hco/1/GRCh38#74602252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154440874-A-C

74602314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440815-C-T

74602320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440809-T-C

74602344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440785-T-C

74602382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440747-C-T

74602386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440743-A-G

74602504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440644-G-A

74602761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440443-A-G

http://identifiers.org/hco/1/GRCh38#74602766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154440435-A-C

74603023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440213-G-A

74603026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440210-C-G

74603188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154440070-G-A

74603395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439913-A-G

74605984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439777-G-A

74605984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439777-G-T

74606103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439696-A-G

74606125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439674-A-G

74606125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439674-A-T

74606210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439597-T-C

74606310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439499-T-C

http://identifiers.org/hco/1/GRCh38#74606390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154439421-C-A

74606390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439421-C-T

74606471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439357-T-G

74606496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439335-G-C

74606496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439335-G-T

74606513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439318-G-A

74606513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154439318-G-T

74606739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154439123-A-T

http://identifiers.org/hco/1/GRCh38#74606804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154439058-C-A

74606813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154439049-T-C

74606954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438906-T-C

74606954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438906-T-G

74606976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438874-G-T

http://identifiers.org/hco/1/GRCh38#74606984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154438866-C-A

74606984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438866-C-T

74606985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438865-T-A

74606985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438865-T-C

74606985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438865-T-G

74607244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438514-T-C

74607506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438111-A-G

74607528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438093-G-A

74607597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154438012-C-T

74608602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437554-C-T

74608743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437414-C-G

74608771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437388-C-T

74608792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437367-G-A

74608792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437367-G-C

74608875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437284-T-C

74609067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154437100-G-A

74609894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436206-T-C

74609968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436133-T-C

74609978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436123-G-A

74609978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154436123-G-T

74612345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433431-C-T

http://identifiers.org/hco/1/GRCh38#74612359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154433417-A-C

74612533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433291-A-T

http://identifiers.org/hco/1/GRCh38#74612584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154433250-C-A

74612584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433250-C-T

74612592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433246-G-A

74612592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433246-G-T

74612605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433231-G-A

74612605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 154433231-G-C

74612806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154433032-G-A

74612806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154433032-G-T

74613578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154432618-A-G

http://identifiers.org/hco/1/GRCh38#74613592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154432604-C-A

http://identifiers.org/hco/1/GRCh38#74613799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154432440-A-C

74613799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154432440-A-T

74614759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154431849-C-T

74614856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154431765-G-C

74614885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154431730-G-T

74615168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154431221-T-C

74615213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 154431177-T-C

74615244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 154431146-A-G

74615244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 154431146-A-T

http://identifiers.org/hco/1/GRCh38#74615268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154431122-A-C

74615368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154431017-G-T

74615882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154430352-A-G

74615948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154430288-G-A

74618432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154428136-A-T

74618439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154428129-C-G

74619041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154427551-C-T

74619052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154427540-A-G

74619072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154427521-T-C

http://identifiers.org/hco/1/GRCh38#74619120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154427474-A-C

74619120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154427474-A-T

74619826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426774-G-A

http://identifiers.org/hco/1/GRCh38#74620005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426622-C-A

74620005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426622-C-G

74620053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426581-G-T

http://identifiers.org/hco/1/GRCh38#74620514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426128-C-A

74620520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426122-A-G

http://identifiers.org/hco/1/GRCh38#74620620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426022-C-A

74620620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426022-C-G

74620620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426022-C-T

http://identifiers.org/hco/1/GRCh38#74620624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154426018-A-C

74620624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426018-A-G

74620627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154426015-T-C

74620682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425960-A-T

74620684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425958-C-G

74620694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425948-A-G

74620726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 154425922-A-G

74620857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 154425791-A-G

74620981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425671-T-A

74620981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425671-T-C

74621007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425645-T-A

74621007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425645-T-C

http://identifiers.org/hco/1/GRCh38#74621044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154425610-C-A

http://identifiers.org/hco/1/GRCh38#74621264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154425444-C-A

74621371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425344-G-A

74621371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425344-G-T

74621382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 154425335-C-T

http://identifiers.org/hco/1/GRCh38#74621412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154425305-C-A

74621442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 154425272-G-T

74621456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 154425260-T-G

74630706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154422492-T-C

74630811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154422419-C-T

http://identifiers.org/hco/1/GRCh38#74631013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154422226-A-C

74631253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154421980-A-G

74631282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154421951-C-T

74631451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154421796-G-T

74631574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154421675-T-A

74631628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419811-A-G

74631628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419811-A-T

74631674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419765-G-T

74631678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419761-T-A

74631678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419761-T-C

74631691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419748-G-C

74631691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419748-G-T

74631975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419464-G-T

http://identifiers.org/hco/1/GRCh38#74632065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154419371-C-A

74632065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419371-C-T

74632303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419186-T-C

74632433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419084-T-A

74632477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419040-G-A

74632505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154419019-C-T

74632853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154418661-G-A

74633202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154418299-A-G

74633302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154418228-T-G

74633456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154418088-T-C

74633725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154417861-T-C

http://identifiers.org/hco/1/GRCh38#74633899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154417725-C-A

74634112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154417522-A-G

74634228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154417422-G-A

74634230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 154417420-A-G

74634701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 154416929-C-T

74634719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 154416911-T-C

74634745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154416885-G-A

74634754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154416876-G-A

74634765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154416865-G-A

74634765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154416865-G-T

74634811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154416819-G-T

74634874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416757-A-G

74634970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416659-T-C

http://identifiers.org/hco/1/GRCh38#74634982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154416648-C-A

74634982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416648-C-T

74635013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416615-T-C

http://identifiers.org/hco/1/GRCh38#74635418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154416296-C-A

74635418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416296-C-T

74635475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416252-T-C

74635530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416193-A-G

74635634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416099-T-C

74635721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154416014-G-A

74635773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415962-G-A

74635788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415948-C-G

74635788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415948-C-T

74636120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415642-A-G

http://identifiers.org/hco/1/GRCh38#74636136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154415627-A-C

74636188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415575-T-A

http://identifiers.org/hco/1/GRCh38#74636224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154415544-C-A

74636224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415544-C-G

http://identifiers.org/hco/1/GRCh38#74636351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154415416-C-A

74636351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154415416-C-T

74636366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154415400-G-A

74636450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415316-G-A

74636450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415316-G-T

74636583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415183-A-G

74636691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154415076-T-G

74636882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154414891-T-C

74636886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154414887-C-G

74637057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154414716-C-T

http://identifiers.org/hco/1/GRCh38#74637297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154414474-C-A

74637373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154414394-T-C

74638457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154413637-G-C

http://identifiers.org/hco/1/GRCh38#74638623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154413483-C-A

74638758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154413353-A-G

74638764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154413347-G-T

74638953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154413163-G-A

http://identifiers.org/hco/1/GRCh38#74638956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154413160-C-A

74638956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154413160-C-G

74639085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154412749-T-C

74639129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154412666-G-T

74639132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154412665-C-G

http://identifiers.org/hco/1/GRCh38#74639254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154412560-C-A

74639482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154412332-A-T

74639489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154412325-A-G

74639772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154412041-G-T

74640282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154411618-C-T

74640366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154411528-T-C

74640657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154411225-C-T

74640885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154411020-T-C

74641057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154410876-G-A

74641349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: synonymous variant
orthologous variants: 154410570-A-G

74641525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154410394-C-T

74641569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154410352-T-A

74641569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154410352-T-C

74641732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154410173-G-A

74641752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154410153-G-A

74641936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409993-C-T

74641942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409988-T-C

74642002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409922-C-T

74642023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409904-G-C

74642218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409712-T-C

74642268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409662-A-G

74642268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409662-A-T

74642296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409634-A-G

74642829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409106-G-C

74642864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409072-T-A

74642874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409066-G-T

74642875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409065-G-T

http://identifiers.org/hco/1/GRCh38#74642910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154409027-C-A

74642920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154409015-T-C

74642982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408958-A-G

74642994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408946-T-C

74642996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408944-T-C

74642997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408943-G-A

74642997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408943-G-C

74642997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408943-G-T

74643216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408751-T-G

74643248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408719-G-A

74643248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408719-G-T

74643374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408594-A-G

74643425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408540-C-T

74643474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408501-G-A

74643518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154408461-A-G

http://identifiers.org/hco/1/GRCh38#74643946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154407310-C-A

74644126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154407141-A-G

74644133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154407135-C-G

74644197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154407084-C-G

http://identifiers.org/hco/1/GRCh38#74644213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154407069-A-C

74644213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154407069-A-G

74644213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154407069-A-T

74644317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154406963-T-C

74644339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154406951-C-T

74644527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154406792-T-C

74644859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154406516-C-T

74645184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154406235-G-T

74645391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154406050-C-T

74645640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154405313-G-A

74646704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154404348-A-G

74646730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: synonymous variant
orthologous variants: 154404322-A-G

74646730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154404322-A-T

http://identifiers.org/hco/1/GRCh38#74646785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154404267-C-A

74646785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154404267-C-T

74646863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404167-A-G

74646863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404167-A-T

74646865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404165-G-A

74646865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404165-G-T

74646878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404146-G-T

74646935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404025-G-A

74646935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404025-G-C

74646935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154404025-G-T

74646966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403994-G-A

http://identifiers.org/hco/1/GRCh38#74646970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154403990-A-C

74646970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403990-A-G

74646984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403976-G-A

74647259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403697-T-C

74647297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403668-T-C

74647332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403624-A-T

74647593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154403304-G-A

74648022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154402648-T-C

74648123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154402558-A-G

74648300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154402397-A-G

74648472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154402225-C-T

74648805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401900-G-T

74648832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401841-C-T

74649078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401613-C-T

http://identifiers.org/hco/1/GRCh38#74649142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154401546-C-A

74649142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401546-C-T

74649150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401539-A-T

74649171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401517-T-C

74649207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401481-T-A

74649207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401481-T-G

74649256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154401433-G-A

74649256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154401433-G-C

74649256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: missense variant
orthologous variants: 154401433-G-T

74649396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401294-T-C

74649402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401288-A-G

http://identifiers.org/hco/1/GRCh38#74649408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154401282-A-C

74649453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154401230-A-G

http://identifiers.org/hco/1/GRCh38#74649467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154401206-C-A

74649935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154400869-G-A

74650170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154400633-T-C

http://identifiers.org/hco/1/GRCh38#74651281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154399922-C-A

74651281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154399922-C-T

http://identifiers.org/hco/1/GRCh38#74651438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154399766-C-A

74651502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154399702-T-C

74651694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154399509-C-T

74651698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154399505-T-A

74651782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154399420-T-A

74652228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154398873-T-C

74652320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154398787-G-A

74652411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154398680-G-A

74652411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154398680-G-C

74652438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154398550-A-T

74653330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397769-C-G

74653361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397744-C-T

74653552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397611-G-A

74653650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397530-A-G

74653837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397359-G-A

74653837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397359-G-C

74654011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397186-A-G

74654066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154397116-T-C

74656554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389507-A-T

74656557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389504-C-G

74656603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389469-T-G

74656669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389401-T-C

74656718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389353-A-T

74656760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389310-G-A

74656765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389305-G-T

74656868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389216-A-G

http://identifiers.org/hco/1/GRCh38#74656919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154389183-C-A

74657035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154389096-A-T

http://identifiers.org/hco/1/GRCh38#74657075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154389052-C-A

74657310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154388844-G-T

74657476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154388641-A-G

74657507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154388609-A-T

74658121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154387962-A-G

74658173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154387937-T-A

74658559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384815-T-C

74658657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384726-C-T

http://identifiers.org/hco/1/GRCh38#74658738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154384461-C-A

http://identifiers.org/hco/1/GRCh38#74658822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154384372-A-C

74659022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384178-C-T

74659025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384175-T-C

74659080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384112-T-C

74659143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384051-C-T

74659144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154384050-T-G

74659355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154383880-C-T

74659442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154383801-A-T

74659532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154383729-C-G

74659564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154383703-A-G

74659724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154383075-C-T

http://identifiers.org/hco/1/GRCh38#74659804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154383032-C-A

74660398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154382852-A-T

74660448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154382804-T-G

74660500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154382752-T-C

74660500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154382752-T-G

http://identifiers.org/hco/1/GRCh38#74661765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154382040-C-A

74661765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154382040-C-T

74661779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154382012-G-A

74661997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154381332-G-A

http://identifiers.org/hco/1/GRCh38#74662049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154381272-C-A

74662060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154381266-T-G

74662359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154380838-A-G

http://identifiers.org/hco/1/GRCh38#74662759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154380497-A-C

74662762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154380494-C-T

74663263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154380193-A-G

74663544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154379896-G-A

74663697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154379777-T-C

74663715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154379759-G-A

http://identifiers.org/hco/1/GRCh38#74663757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154379696-C-A

74664331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378595-T-A

74664335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378591-T-G

74664336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378590-A-G

74664500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378425-T-C

74664518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378407-G-T

74664627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378298-T-C

74664734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378185-C-T

74664782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378137-C-T

74664803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154378116-T-C

http://identifiers.org/hco/1/GRCh38#74664889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154377853-C-A

74665052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154377511-G-A

74665061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154377502-G-C

74665233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154377365-G-C

74665244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154377354-A-G

74665314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154377285-T-C

74665373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154377240-A-G

74665623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154376235-G-A

74665732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154376102-T-C

74666241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154375322-A-G

http://identifiers.org/hco/1/GRCh38#74666491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154375082-C-A

74666492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154375081-T-C

74666612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374985-G-A

74667096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374634-T-A

74667284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374448-T-C

74667427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374306-G-A

74667427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374306-G-T

74667472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374263-G-A

74667613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374131-C-G

74667631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374113-A-G

74667632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374112-T-C

74667649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374093-T-C

74667678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154374065-G-A

74668464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154373531-T-C

74668530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154373484-C-G

74668579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154373434-C-G

74668676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154373345-A-G

74669003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154373047-G-A

74669324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372886-T-G

74669461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372743-G-T

74669475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372730-T-G

74669488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372716-T-C

74669560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372650-T-C

74669560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372650-T-G

74669723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372496-T-A

74669734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372484-T-A

74669747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154372471-G-A

74670243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154371820-G-A

74671985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154371314-T-G

74672016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154371292-T-G

74672139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154371167-T-C

74672259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154371049-C-T

74672675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370725-A-G

74672765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370629-C-G

74672808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370588-G-A

74672995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370412-G-A

74673019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370391-A-G

74673182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370232-A-G

74673219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370194-G-A

74673272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370140-G-A

74673302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370112-G-A

74673379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370036-C-G

http://identifiers.org/hco/1/GRCh38#74673383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154370031-C-A

74673383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154370031-C-T

http://identifiers.org/hco/1/GRCh38#74673400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154370014-C-A

74673428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369987-G-A

74673428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369987-G-C

74673428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369987-G-T

74673453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369960-G-A

74673556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369859-G-A

74673556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369859-G-T

74673584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369847-C-T

74673593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369839-T-A

74673593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369839-T-G

74673615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369825-T-C

74673615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369825-T-G

74673664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369801-G-A

74673664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369801-G-T

http://identifiers.org/hco/1/GRCh38#74673711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154369757-C-A

74673711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369757-C-T

74673712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369756-T-A

74673712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369756-T-C

74673713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369755-C-G

74673713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369755-C-T

74673776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369692-G-A

74673776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369692-G-T

http://identifiers.org/hco/1/GRCh38#74673791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154369677-C-A

74673791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369677-C-G

74673791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 154369677-C-T

http://identifiers.org/hco/1/GRCh38#74673802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154369666-C-A

74673802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369666-C-T

http://identifiers.org/hco/1/GRCh38#74673848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154369620-C-A

74673879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369579-T-C

74673879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369579-T-G

74673880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369578-G-A

74673880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: 154369578-G-T

http://identifiers.org/hco/1/GRCh38#74673881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#154369577-C-A

74674272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, undefined
orthologous variants: 154369178-G-A

74674273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, undefined
orthologous variants: 154369177-A-G

74674274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25346
most severe consequence: intron_variant, undefined
orthologous variants: 154369176-C-T