http://identifiers.org/hco/10/GRCh38#132808638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139180966-C-A

132808655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 139180982-G-A

132808655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 139180982-G-T

132808677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 139181004-T-A

132808730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 139181035-G-A

132808785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 139181073-G-A

132808785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 139181073-G-T

http://identifiers.org/hco/10/GRCh38#132808797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139181079-C-A

132808797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense variant
orthologous variants: 139181079-C-G

132808797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense variant
orthologous variants: 139181079-C-T

http://identifiers.org/hco/10/GRCh38#132808873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139181164-C-A

132808873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 139181164-C-T

132808903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: splice_region_variant, stop_gained, synonymous_variant
orthologous variants: 139181194-G-A

132808903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, splice_region_variant, synonymous_variant
orthologous variants: 139181194-G-T

132808913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181203-A-G

132808914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181204-A-G

132808945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181238-G-A

132808945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181238-G-T

http://identifiers.org/hco/10/GRCh38#132808996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139181313-C-A

132808996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181313-C-T

132808998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181315-G-A

132808998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181315-G-C

132808998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139181315-G-T

132810318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183035-G-C

132810318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183035-G-T

http://identifiers.org/hco/10/GRCh38#132810330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183046-C-A

132810330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183046-C-T

http://identifiers.org/hco/10/GRCh38#132810340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183056-C-A

132810340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183056-C-G

132810340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183056-C-T

132810400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183105-C-G

132810449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 139183151-A-G

132810449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 139183151-A-T

132810494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139183196-G-A

132810563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183280-G-A

132810563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron variant
orthologous variants: 139183280-G-T

http://identifiers.org/hco/10/GRCh38#132810645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183364-C-A

132810645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant
orthologous variants: 139183364-C-T

132810658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 139183377-G-T

http://identifiers.org/hco/10/GRCh38#132810739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183451-C-A

http://identifiers.org/hco/10/GRCh38#132810770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183481-C-A

132810770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183481-C-G

132810770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183481-C-T

http://identifiers.org/hco/10/GRCh38#132810772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183483-C-A

132810772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183483-C-G

132810772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183483-C-T

http://identifiers.org/hco/10/GRCh38#132810796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183496-C-A

132810796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183496-C-T

132810800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183500-G-A

132810800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183500-G-T

http://identifiers.org/hco/10/GRCh38#132810840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183539-C-A

132810840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183539-C-G

132810840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183539-C-T

132810847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183545-G-T

http://identifiers.org/hco/10/GRCh38#132810857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183602-C-A

132810857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183602-C-G

132810857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183602-C-T

132810895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183707-G-A

132810895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183707-G-C

http://identifiers.org/hco/10/GRCh38#132810928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183757-C-A

132810928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 139183757-C-T

132810964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139183806-G-A

132810964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139183806-G-T

132810972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139183814-T-C

132810972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139183814-T-G

http://identifiers.org/hco/10/GRCh38#132811058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139183900-C-A

132811058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139183900-C-T

132811179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183975-A-G

132811181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183977-G-C

132811181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139183977-G-T

132811394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184127-G-A

132811788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184566-T-C

132811788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184566-T-G

132811844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184614-T-C

132811949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184711-C-G

132811963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184727-G-T

132812126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184898-C-T

132812151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184923-G-A

132812151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139184923-G-C

132812394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185155-G-A

132812501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185237-A-T

132812651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185369-G-T

132812663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185376-G-A

132812663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185376-G-C

132812663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185376-G-T

132812666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185379-G-A

132812676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185389-G-T

132812704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185422-G-C

132812704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185422-G-T

http://identifiers.org/hco/10/GRCh38#132812748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139185465-C-A

132812748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185465-C-T

132812771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185495-A-G

132812906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185630-A-G

132812929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185653-G-A

132812929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139185653-G-T

http://identifiers.org/hco/10/GRCh38#132814310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139186680-C-A

132814310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186680-C-T

http://identifiers.org/hco/10/GRCh38#132814323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139186699-C-A

132814323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186699-C-T

132814324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186700-C-T

http://identifiers.org/hco/10/GRCh38#132814336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139186712-C-A

http://identifiers.org/hco/10/GRCh38#132814377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139186795-C-A

132814377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186795-C-T

http://identifiers.org/hco/10/GRCh38#132814496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139186906-C-A

132814496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186906-C-T

132814514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186924-G-A

132814514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186924-G-T

132814529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186939-G-A

132814529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139186939-G-T

132814579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139186997-G-A

132814579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139186997-G-T

132814585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139187003-T-A

132814585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139187003-T-C

132814585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139187003-T-G

132814596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139187014-G-A

132814596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139187014-G-T

132814616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139187034-G-C

132814616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139187034-G-T

132814705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139187125-G-A

132814705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139187125-G-C

132814756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187189-C-T

132814799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187221-C-T

132814816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187235-C-G

132814816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187235-C-T

http://identifiers.org/hco/10/GRCh38#132814833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139187248-C-A

132814833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187248-C-T

132815057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187462-G-A

132815057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187462-G-T

http://identifiers.org/hco/10/GRCh38#132815069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139187466-C-A

132815069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187466-C-T

132815149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187537-G-A

http://identifiers.org/hco/10/GRCh38#132815175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139187555-C-A

132815175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187555-C-G

132815271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187640-C-G

132815271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187640-C-T

132815288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187668-A-G

132815302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187682-T-C

132815353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187727-C-T

132815446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187814-G-A

http://identifiers.org/hco/10/GRCh38#132815447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139187815-C-A

132815448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139187816-T-C

132833416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139191951-A-G

132833528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139192054-G-A

http://identifiers.org/hco/10/GRCh38#132833633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139192174-C-A

132833633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139192174-C-T

http://identifiers.org/hco/10/GRCh38#132833638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139192179-C-A

132833638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139192179-C-T

132833918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139193273-G-A

132833918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139193273-G-T

http://identifiers.org/hco/10/GRCh38#132833946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139193332-C-A

132833946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139193332-C-G

132833946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139193332-C-T

http://identifiers.org/hco/10/GRCh38#132833996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139193386-C-A

132833996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139193386-C-T

132834059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139193440-T-C

132834681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139194350-A-G

132834775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139194441-C-G

132834775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139194441-C-T

132834844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194523-G-A

132834844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194523-G-T

132834848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194527-C-T

http://identifiers.org/hco/10/GRCh38#132834866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194544-C-A

132834866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194544-C-T

132834919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194594-G-C

132834919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194594-G-T

http://identifiers.org/hco/10/GRCh38#132834924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194599-C-A

132834924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194599-C-T

http://identifiers.org/hco/10/GRCh38#132834926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194601-A-C

132834926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194601-A-T

http://identifiers.org/hco/10/GRCh38#132834966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194653-C-A

132834966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194653-C-T

132835020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194713-C-G

http://identifiers.org/hco/10/GRCh38#132835063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194756-C-A

http://identifiers.org/hco/10/GRCh38#132835165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194831-C-A

132835165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194831-C-T

http://identifiers.org/hco/10/GRCh38#132835233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194876-C-A

http://identifiers.org/hco/10/GRCh38#132835234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194877-A-C

132835243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194886-G-A

http://identifiers.org/hco/10/GRCh38#132835271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194911-C-A

132835271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194911-C-T

132835295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139194933-G-A

http://identifiers.org/hco/10/GRCh38#132835302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139194940-A-C

132835302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 139194940-A-T

132835317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139194954-A-G

132835378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139195015-C-G

132835378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139195015-C-T

http://identifiers.org/hco/10/GRCh38#132835454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195085-C-A

http://identifiers.org/hco/10/GRCh38#132835456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195087-C-A

132835479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195110-G-A

132835488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195119-T-G

132835489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195120-G-T

132835500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195138-G-T

132835525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195169-G-A

132835525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195169-G-T

http://identifiers.org/hco/10/GRCh38#132835535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195179-A-C

132835535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195179-A-T

http://identifiers.org/hco/10/GRCh38#132835775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195318-A-C

132835775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195318-A-G

132835900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195360-C-T

132835902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195362-C-T

http://identifiers.org/hco/10/GRCh38#132836287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195624-A-C

http://identifiers.org/hco/10/GRCh38#132836305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195640-C-A

132836307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195642-G-T

132836308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195643-T-A

http://identifiers.org/hco/10/GRCh38#132836672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195944-C-A

132836672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195944-C-T

http://identifiers.org/hco/10/GRCh38#132836676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195948-C-A

http://identifiers.org/hco/10/GRCh38#132836711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139195986-C-A

132836711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195986-C-T

132836723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195999-G-C

132836723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139195999-G-T

132836805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196081-G-C

132836854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139196129-T-C

132837157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196334-T-G

132838122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196475-C-G

132838122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196475-C-T

132838162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196507-C-T

132838193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196538-C-T

132838304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196618-T-C

132838383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196696-C-T

http://identifiers.org/hco/10/GRCh38#132838389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139196702-C-A

132838389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196702-C-G

132838390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196703-G-A

132838397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196710-G-C

132838446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139196759-T-C

http://identifiers.org/hco/10/GRCh38#132846075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139197366-C-A

132846075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139197366-C-G

132846075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139197366-C-T

132846240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197531-A-G

132846282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197551-T-C

132846390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197581-C-T

132846391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197582-G-A

132846723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197740-C-T

132846726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197743-T-G

132846736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197752-C-T

132846737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139197753-G-A

132847009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139198073-C-T

132847016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198080-G-A

132847016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198080-G-T

132847088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139198152-C-G

132847088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198152-C-T

132847094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198158-G-A

http://identifiers.org/hco/10/GRCh38#132847135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139198201-C-A

132847135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139198201-C-T

132847183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139198250-G-A

132847183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139198250-G-C

132847196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198265-C-T

132847263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139198326-G-A

132847263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139198326-G-C

132847277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198340-T-C

132847292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139198355-A-G

132847383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139198446-G-A

132847383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139198446-G-T

132850208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139199802-T-C

http://identifiers.org/hco/10/GRCh38#132850415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139200009-C-A

132850453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139200051-T-C

132850475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139200076-A-G

http://identifiers.org/hco/10/GRCh38#132850477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139200078-C-A

132850477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139200078-C-T

132850552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139200136-A-G

132850556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139200142-A-G

132850606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139200220-A-G

132851078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139201061-G-A

132851078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139201061-G-C

132851120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139201112-G-C

132851333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139201344-C-G

132851333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139201344-C-T

http://identifiers.org/hco/10/GRCh38#132851388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139201380-A-C

132857801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207402-T-A

132857845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207470-T-A

132857850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207475-T-C

132857850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207475-T-G

132857882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207511-G-C

132857893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207522-G-C

132857893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207522-G-T

132857895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139207526-T-C

132859061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209641-G-A

132859169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139209749-C-T

132859183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139209763-A-G

http://identifiers.org/hco/10/GRCh38#132859270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139209852-C-A

132859270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 139209852-C-T

http://identifiers.org/hco/10/GRCh38#132859278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139209861-C-A

132859278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139209861-C-T

http://identifiers.org/hco/10/GRCh38#132859298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139209884-C-A

132859298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209884-C-T

132859305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209891-T-C

132859305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209891-T-G

132859314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209900-G-A

132859314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209900-G-C

132859314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209900-G-T

http://identifiers.org/hco/10/GRCh38#132859362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139209955-C-A

132859362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209955-C-T

132859368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209961-G-A

132859368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209961-G-T

132859402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139209987-C-T

132860303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139210392-A-G

132860344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139210427-A-G

132860467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139210544-T-G

132860798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139210730-G-A

132860798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139210730-G-C

132866214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212118-G-T

132866277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212163-A-G

132866387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212247-T-C

132866655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212434-G-A

132866780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212506-T-A

132866780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212506-T-C

132866788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212514-C-T

132866910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212640-G-A

http://identifiers.org/hco/10/GRCh38#132867032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139212798-C-A

132867032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212798-C-T

132867094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212865-C-T

http://identifiers.org/hco/10/GRCh38#132867095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139212866-A-C

132867095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212866-A-G

132867117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139212889-G-C

132867414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139213176-G-T

132867426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139213188-C-T

132867462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139213224-A-G

http://identifiers.org/hco/10/GRCh38#132867477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139213239-C-A

132867477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139213239-C-T

132867622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213390-T-A

132867622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213390-T-C

132867622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213390-T-G

132867626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213394-T-C

http://identifiers.org/hco/10/GRCh38#132867628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139213409-C-A

132867628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213409-C-G

132867628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213409-C-T

132867669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213441-A-G

132867765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213524-C-T

132867766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213525-G-A

132868049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213713-G-A

132868165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213820-C-T

132868180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213827-T-G

132868279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213889-G-A

132868313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213925-T-C

132868323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139213935-A-T

132868900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214547-G-C

132869065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214754-G-A

http://identifiers.org/hco/10/GRCh38#132869165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139214848-C-A

132869165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214848-C-T

132869217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214905-G-A

132869217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214905-G-T

132869233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214928-A-G

132869233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214928-A-T

132869241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214936-A-G

132869251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214942-G-A

132869251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139214942-G-T

132869294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139214981-G-A

132869294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139214981-G-T

http://identifiers.org/hco/10/GRCh38#132869345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139215032-C-A

132869345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139215032-C-T

132869407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215097-A-G

132869445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215142-G-A

132869445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215142-G-T

http://identifiers.org/hco/10/GRCh38#132869458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139215155-C-A

132869458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215155-C-G

132869458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215155-C-T

132869809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215484-C-T

132872517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139215628-A-G

132872573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139215676-C-T

132873288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139216658-G-A

132876812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 139218195-C-G

132876812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 139218195-C-T

132876827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139218210-T-C

132876869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139218252-A-G

http://identifiers.org/hco/10/GRCh38#132879426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139219459-C-A

132879426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 139219459-C-T

132880896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139220287-G-A

132880896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139220287-G-C

132880922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139220313-G-A

132880922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139220313-G-C

132880922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139220313-G-T

132884183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139221645-C-G

132884183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139221645-C-T

132884436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139221846-G-A

132884436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139221846-G-C

http://identifiers.org/hco/10/GRCh38#132884642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139222043-C-A

132884642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222043-C-G

132884824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222136-C-T

http://identifiers.org/hco/10/GRCh38#132884959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139222227-C-A

132884959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222227-C-G

132884959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222227-C-T

http://identifiers.org/hco/10/GRCh38#132885006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139222249-C-A

132885006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222249-C-T

http://identifiers.org/hco/10/GRCh38#132885009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139222252-C-A

132885009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222252-C-T

132885012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222255-A-G

132885027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222269-A-G

132885069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222311-T-C

132885087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222331-G-A

132885298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222541-G-A

132885298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222541-G-C

132885321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222563-A-T

132885499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222659-G-A

132885690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222690-G-A

132885690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222690-G-T

132885740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222710-G-A

132885808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222739-G-A

132885808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139222739-G-T

http://identifiers.org/hco/10/GRCh38#132885959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139222890-C-A

http://identifiers.org/hco/10/GRCh38#132889026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139223185-C-A

132890040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139224207-T-C

132890901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139224932-G-T

132890918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139224949-C-T

132891071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139225084-C-T

132891079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139225092-T-C

132892290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139225369-C-G

132892290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139225369-C-T

132892300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139225379-G-A

132898917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139226170-G-A

132899034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139226270-G-A

132899034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139226270-G-C

132899034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139226270-G-T

132899109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139226345-G-A

132899109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139226345-G-C

132899133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226399-C-G

132899133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226399-C-T

http://identifiers.org/hco/10/GRCh38#132899134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139226400-A-C

132899147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226438-G-A

132899161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226452-G-A

132899161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226452-G-C

132899184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226481-G-A

132899184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226481-G-T

http://identifiers.org/hco/10/GRCh38#132899254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139226615-C-A

132899254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226615-C-T

132899504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226861-G-A

132899504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139226861-G-C

132899765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227091-A-G

http://identifiers.org/hco/10/GRCh38#132899785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139227104-C-A

132899785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227104-C-T

http://identifiers.org/hco/10/GRCh38#132899794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139227113-A-C

132899876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227168-G-A

132899978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227289-C-G

132900429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227746-C-T

http://identifiers.org/hco/10/GRCh38#132900453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139227767-A-C

http://identifiers.org/hco/10/GRCh38#132900550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139227864-A-C

132900595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227901-G-A

132900641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139227945-G-A

132904418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139228146-C-T

http://identifiers.org/hco/10/GRCh38#132907246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139229390-C-A

132907268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139229414-C-T

132908503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139230738-C-T

132908642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139230878-T-C

132908642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139230878-T-G

http://identifiers.org/hco/10/GRCh38#132908664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139230900-C-A

132908664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139230900-C-T

132908718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139230969-G-A

132908718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139230969-G-C

132908718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139230969-G-T

http://identifiers.org/hco/10/GRCh38#132908745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139231011-C-A

132908757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231023-A-T

132909028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231333-G-A

132909028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231333-G-T

132909078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231383-G-A

132909078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231383-G-C

132909078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231383-G-T

132909125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231443-G-A

132909125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231443-G-T

132909255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231573-G-T

132909274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231587-G-A

132909274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231587-G-T

132909327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231661-A-G

132909391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231724-A-G

132909469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231798-G-C

http://identifiers.org/hco/10/GRCh38#132909596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139231978-C-A

132909596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139231978-C-T

132909712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232144-C-T

http://identifiers.org/hco/10/GRCh38#132909899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139232280-A-C

132909899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232280-A-G

132909899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232280-A-T

http://identifiers.org/hco/10/GRCh38#132910018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139232412-C-A

132910018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139232412-C-T

132910080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139232474-G-A

132910080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139232474-G-T

http://identifiers.org/hco/10/GRCh38#132912621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139232537-C-A

132912621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232537-C-T

http://identifiers.org/hco/10/GRCh38#132912631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139232547-C-A

132912631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232547-C-G

132912631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232547-C-T

http://identifiers.org/hco/10/GRCh38#132912635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139232551-C-A

132912635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139232551-C-T

132912824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139232743-G-A

132912824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139232743-G-C

http://identifiers.org/hco/10/GRCh38#132913046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139233311-C-A

132913060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139233325-G-T

132913159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139233424-G-A

132913159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139233424-G-C

132916544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139234474-C-T

http://identifiers.org/hco/10/GRCh38#132916572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139234502-C-A

132916572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139234502-C-T

http://identifiers.org/hco/10/GRCh38#132916590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139234520-C-A

132916590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139234520-C-T

132916710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139234665-G-C

132916710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139234665-G-T

132916714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139234669-T-C

132916717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139234672-G-A

132918385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139235714-T-A

132918385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139235714-T-C

132918385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139235714-T-G

http://identifiers.org/hco/10/GRCh38#132918456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139235785-C-A

132918456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139235785-C-T

http://identifiers.org/hco/10/GRCh38#132918465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139235794-C-A

132918465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139235794-C-T

132918552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139235876-T-A

132918552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139235876-T-G

http://identifiers.org/hco/10/GRCh38#132919266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139236441-A-C

132919951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237038-C-T

132919995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237081-G-A

132919995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237081-G-T

132919999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237085-T-C

132919999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237085-T-G

132920029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237127-G-A

132920029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237127-G-T

http://identifiers.org/hco/10/GRCh38#132920049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139237169-C-A

132920049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139237169-C-T

http://identifiers.org/hco/10/GRCh38#132920172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139237292-C-A

132920172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139237292-C-T

http://identifiers.org/hco/10/GRCh38#132922053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240462-C-A

132922053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240462-C-T

132922079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240486-T-C

132922086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240492-G-A

132922086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240492-G-C

132922086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240492-G-T

132922276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240666-C-T

132922293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240678-A-G

http://identifiers.org/hco/10/GRCh38#132922298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240683-C-A

132922298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240683-C-G

132922298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240683-C-T

http://identifiers.org/hco/10/GRCh38#132922299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240684-C-A

http://identifiers.org/hco/10/GRCh38#132922316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240700-C-A

132922316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240700-C-T

132922332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240711-G-T

132922349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240725-C-T

132922366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240740-T-G

132922390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240767-G-A

132922390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240767-G-T

http://identifiers.org/hco/10/GRCh38#132922396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240776-C-A

132922396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240776-C-T

132922443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240856-G-A

132922443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240856-G-T

http://identifiers.org/hco/10/GRCh38#132922458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240861-C-A

132922458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240861-C-T

http://identifiers.org/hco/10/GRCh38#132922468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240871-C-A

132922468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139240871-C-T

132922472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139240875-G-T

http://identifiers.org/hco/10/GRCh38#132922552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240955-C-A

132922552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139240955-C-G

132922552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139240955-C-T

http://identifiers.org/hco/10/GRCh38#132922580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139240983-C-A

132922580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139240983-C-T

132922603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139241006-G-T

132922605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139241008-G-A

132922605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139241008-G-T

http://identifiers.org/hco/10/GRCh38#132924722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139246132-A-C

132924785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139246195-G-A

132924785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139246195-G-T

132924842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139246252-T-C

132924924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246327-G-A

132924924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246327-G-T

132924925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246328-G-A

132924925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246328-G-C

132924925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246328-G-T

132924930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246333-A-G

132924931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246334-G-A

132924931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246334-G-T

132924936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246339-G-A

132924936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246339-G-T

132924980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246421-G-A

132924980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246421-G-T

132925034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246477-G-A

132925034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246477-G-T

http://identifiers.org/hco/10/GRCh38#132925302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139246725-C-A

132925302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246725-C-T

132925327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139246746-G-A

132926592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139246899-T-C

132926727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139247032-T-C

132929371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139255591-T-C

132929400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139255614-G-T

132929407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139255621-T-C

http://identifiers.org/hco/10/GRCh38#132929412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139255626-C-A

132929498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139255710-A-G

132929498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 139255710-A-T

http://identifiers.org/hco/10/GRCh38#132929542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139255754-C-A

132929545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 139255757-C-T

132929639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 139255815-C-T

http://identifiers.org/hco/10/GRCh38#132929802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139255980-A-C

132929802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139255980-A-G

132929802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139255980-A-T

132929814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139255992-A-G

132934569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258238-C-G

132934569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258238-C-T

http://identifiers.org/hco/10/GRCh38#132934609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139258282-A-C

http://identifiers.org/hco/10/GRCh38#132934625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139258298-C-A

http://identifiers.org/hco/10/GRCh38#132934661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139258334-C-A

132934831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139258485-T-C

132934879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258533-G-T

132934894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258539-A-G

132934894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258539-A-T

http://identifiers.org/hco/10/GRCh38#132934960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139258613-C-A

132934960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258613-C-T

132934970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258623-G-A

132934970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258623-G-T

132935055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258710-C-G

132935115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258772-T-G

132936580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258906-C-T

132936657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139258980-T-C

132936782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259103-T-A

132936842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259158-T-C

http://identifiers.org/hco/10/GRCh38#132936850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139259166-C-A

132936850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259166-C-T

132936890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259201-A-G

132936999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139259279-A-G

132937001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139259281-T-C

132937005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139259285-A-G

http://identifiers.org/hco/10/GRCh38#132937026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139259306-C-A

132937026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139259306-C-G

132937030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139259310-A-G

132937030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139259310-A-T

132937069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259348-G-A

132937069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259348-G-T

132937080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259359-T-A

132937080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139259359-T-C

132937115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259386-T-G

132937130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259401-T-G

132937237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259542-G-A

132937237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259542-G-T

132937258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259561-G-T

132937333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259627-A-T

132937424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139259684-G-T

http://identifiers.org/hco/10/GRCh38#132937772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139260030-C-A

132937827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260082-G-A

132937827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260082-G-T

132937871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260124-T-C

132937879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260168-G-C

132937931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260224-C-T

132937932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260225-G-A

132938034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260314-C-T

http://identifiers.org/hco/10/GRCh38#132938043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139260324-C-A

132938060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260341-G-A

132938192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260412-C-T

132938199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260419-G-A

132938425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260632-T-C

132938522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260713-G-A

132938522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260713-G-T

132938541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260718-A-G

132938578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260727-G-T

132938642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 139260791-G-A

132938642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139260791-G-T

132938678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139260827-A-G

132938723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139260872-G-A

132938723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139260872-G-T

132938761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139260910-G-A

132938761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139260910-G-T

132938765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260914-G-T

132938863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139260992-G-A

132938992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139261106-G-A

132938992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139261106-G-C

132939013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139261127-C-G

132939013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139261127-C-T

132939032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139261130-C-G

132939407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139261443-G-A

132940761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262163-G-A

132940871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262271-A-G

132940906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262303-A-G

132940930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262327-T-G

132940931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262328-G-A

132940931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262328-G-T

132940982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262384-T-C

132940982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262384-T-G

132941001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139262402-T-C

http://identifiers.org/hco/10/GRCh38#132941172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139262561-C-A

132941213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262583-G-C

132941395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262724-G-A

132941449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262794-G-A

132941449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139262794-G-T

132941747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263075-G-C

http://identifiers.org/hco/10/GRCh38#132941780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139263092-A-C

132941780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263092-A-T

http://identifiers.org/hco/10/GRCh38#132941811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139263102-C-A

132941811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263102-C-G

132941811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263102-C-T

132941864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263158-G-A

132941864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263158-G-T

http://identifiers.org/hco/10/GRCh38#132941866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139263160-C-A

http://identifiers.org/hco/10/GRCh38#132941900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#139263183-C-A

132941900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263183-C-G

132941900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263183-C-T

132942019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139263301-G-A

132942019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139263301-G-T

132942251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263481-T-C

132942251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139263481-T-G

132942525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139263706-G-A

132942525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139263706-G-T

132942621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139263768-G-A

132942621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139263768-G-T

http://identifiers.org/hco/10/GRCh38#132942641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#139263790-C-A

132942641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25247
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139263790-C-G