132207549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683630-T-C

132207549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683630-T-G

132207664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683761-T-C

132207664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683761-T-G

132207722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683855-A-G

132207722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683855-A-T

132207731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683869-G-A

132207731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683869-G-C

132207731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683869-G-T

132207762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683900-A-T

http://identifiers.org/hco/10/GRCh38#132207798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138683939-C-A

132207798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683939-C-G

132207798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138683939-C-T

132207985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138684107-G-C

132207985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138684107-G-T

http://identifiers.org/hco/10/GRCh38#132207997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138684120-C-A

132207997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138684120-C-G

132207997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 138684120-C-T

132208030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138684159-G-A

132208030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138684159-G-T

http://identifiers.org/hco/10/GRCh38#132208079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138684211-C-A

132208114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138684246-G-A

132208158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138684292-T-C

http://identifiers.org/hco/10/GRCh38#132208205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138684359-C-A

132208205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684359-C-G

132208205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684359-C-T

http://identifiers.org/hco/10/GRCh38#132208215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138684369-A-C

132208215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684369-A-G

132208410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684607-T-C

132208520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684708-C-G

132208520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684708-C-T

132208521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684709-G-A

132208577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684766-C-T

132208650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684841-G-A

132208650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684841-G-T

132208682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684874-G-A

132208684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684876-G-A

132208737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684921-G-T

132208740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684924-G-A

132208753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684930-T-C

132208821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138684989-C-T

132208892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685063-G-A

132208892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685063-G-C

132208892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685063-G-T

http://identifiers.org/hco/10/GRCh38#132208920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138685092-A-C

132208920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685092-A-G

132208920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685092-A-T

http://identifiers.org/hco/10/GRCh38#132208942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138685105-C-A

132208942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685105-C-G

132208942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685105-C-T

132208976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685126-C-G

132208976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685126-C-T

132209122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138685267-G-A

132219684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138691741-C-T

132219799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138691844-C-G

132219799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138691844-C-T

http://identifiers.org/hco/10/GRCh38#132222496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138698790-C-A

132222503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698797-T-A

132222503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698797-T-C

132222508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698802-G-A

132222508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698802-G-T

http://identifiers.org/hco/10/GRCh38#132222575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138698891-C-A

132222575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698891-C-T

132222581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698897-G-A

132222581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698897-G-T

132222582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698898-G-A

132222582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698898-G-T

132222632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698924-G-A

132222632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138698924-G-C

132222683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138698975-G-A

132222683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138698975-G-C

132222716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138699008-G-A

132222716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138699008-G-C

132222716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138699008-G-T

http://identifiers.org/hco/10/GRCh38#132222722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138699014-C-A

132222722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138699014-C-G

132222722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138699014-C-T

132222819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138699110-T-A

132222819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138699110-T-C

132222902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138699198-G-A

132222902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138699198-G-T

132222903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 138699199-G-A

132222903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 138699199-G-T

132222942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138699238-G-A

132222942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138699238-G-C

132222942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138699238-G-T

http://identifiers.org/hco/10/GRCh38#132223028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#138699311-C-A

132223028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699311-C-T

132223033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138699316-G-A

132223033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138699316-G-T

http://identifiers.org/hco/10/GRCh38#132223066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138699348-A-C

http://identifiers.org/hco/10/GRCh38#132223087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#138699369-A-C

132223087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699369-A-G

132223087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699369-A-T

http://identifiers.org/hco/10/GRCh38#132223099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#138699379-A-C

132223099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699379-A-G

132223099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699379-A-T

http://identifiers.org/hco/10/GRCh38#132223112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#138699393-C-A

132223112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699393-C-T

132223136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699417-G-A

132223136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699417-G-T

132223338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 138699587-A-G

132223825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700037-C-T

132223832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700044-C-G

132223832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700044-C-T

132223895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700081-G-A

132223909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700094-T-C

132223910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700095-G-A

132224038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700207-C-T

http://identifiers.org/hco/10/GRCh38#132224065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700238-A-C

132224109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700284-G-A

http://identifiers.org/hco/10/GRCh38#132224128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700311-C-A

132224132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700315-C-T

http://identifiers.org/hco/10/GRCh38#132224255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700437-C-A

132224259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700442-G-A

132224259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700442-G-T

132224318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700489-T-C

132224318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700489-T-G

132224319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700490-G-A

132224319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700490-G-T

132224367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700551-G-A

132224367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700551-G-T

132224393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700572-G-C

132224393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700572-G-T

132224398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700577-G-A

132224398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700577-G-T

132224401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700580-G-A

132224401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700580-G-C

132224401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700580-G-T

http://identifiers.org/hco/10/GRCh38#132224448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700627-C-A

132224448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138700627-C-T

132224449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138700628-A-G

http://identifiers.org/hco/10/GRCh38#132224482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700661-C-A

132224482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138700661-C-T

132224503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138700682-G-A

132224503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138700682-G-C

132224503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138700682-G-T

132224527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138700706-G-A

132224527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138700706-G-C

132224527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138700706-G-T

132224537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700716-G-A

132224537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700716-G-C

132224537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700716-G-T

132224568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700743-G-A

132224568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700743-G-T

http://identifiers.org/hco/10/GRCh38#132224616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700776-C-A

132224616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700776-C-G

132224616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700776-C-T

http://identifiers.org/hco/10/GRCh38#132224625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700785-C-A

132224625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700785-C-G

132224625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700785-C-T

http://identifiers.org/hco/10/GRCh38#132224628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700788-C-A

132224628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700788-C-T

http://identifiers.org/hco/10/GRCh38#132224704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138700854-C-A

132224704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700854-C-T

132224710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700860-G-C

132224757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700933-G-A

132224757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138700933-G-C

132224965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701092-G-T

132225103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701168-T-C

132225148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701193-G-A

132225148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701193-G-T

132225193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701243-G-A

132225193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701243-G-C

132225193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701243-G-T

132225287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138701326-G-A

132225313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 138701352-C-T

132225410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701466-T-C

132225415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701484-G-A

132225425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701494-G-A

132225425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701494-G-C

132225486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701613-G-A

132225503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701658-T-C

132225519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138701669-G-A

132225519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138701669-G-T

132225520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 138701670-G-T

132225534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 138701684-C-T

132225659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701806-A-G

132225679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701817-T-C

132225803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701908-G-A

132225825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701932-C-T

http://identifiers.org/hco/10/GRCh38#132225826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138701933-C-A

132225876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701965-T-A

132225876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701965-T-C

132225898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701979-G-A

132225904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701985-T-C

132225904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138701985-T-G

132226091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702219-C-T

132226146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702286-C-T

132226235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702381-G-T

132226294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702428-A-T

132226346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702468-T-C

132226408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702493-C-T

132226422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702507-T-C

132226436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702521-T-G

132226442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702527-C-T

http://identifiers.org/hco/10/GRCh38#132226463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138702547-C-A

132226522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702579-G-T

132226649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702648-G-T

http://identifiers.org/hco/10/GRCh38#132226680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138702654-C-A

132226680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702654-C-T

132226764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702713-C-G

132226764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138702713-C-T

132226845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
orthologous variants: 138702795-G-A

http://identifiers.org/hco/10/GRCh38#132227035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138702973-C-A

http://identifiers.org/hco/10/GRCh38#132227113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138703013-A-C

132227113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703013-A-G

http://identifiers.org/hco/10/GRCh38#132227340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138703221-C-A

132227340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703221-C-T

132227472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703337-G-A

132227534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703389-T-C

132227598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138703453-G-C

132227833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704909-A-G

132227867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704941-C-G

132227867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704941-C-T

132227883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704956-G-T

132227941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704996-G-A

132227941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704996-G-C

132227941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138704996-G-T

132228157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 138705224-C-T

132228622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705397-G-C

132228671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138705447-C-T

http://identifiers.org/hco/10/GRCh38#132229663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138709605-C-A

132229747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138709662-G-A

http://identifiers.org/hco/10/GRCh38#132229931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138709862-A-C

132229969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138709889-G-A

132229969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138709889-G-C

132229991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138709897-T-G

132230162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710043-G-A

132230232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710140-G-A

132230301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138710222-C-T

132233033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711933-T-A

132233033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711933-T-C

132233081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711950-G-A

132233117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138711989-C-T

132237364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715216-G-A

132237540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715371-T-C

132237589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715418-A-G

132237710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715524-C-T

http://identifiers.org/hco/10/GRCh38#132237849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138715671-C-A

132237849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715671-C-T

132237879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715696-C-T

132237933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715730-T-A

132238035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715797-G-C

http://identifiers.org/hco/10/GRCh38#132238060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138715820-C-A

132238069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138715829-G-A

132239228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138716125-C-T

132239340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138716210-T-C

132239537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138716390-C-T

132239777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138716688-G-A

132239785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138716696-T-C

132239802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138716717-G-A

132240302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717154-G-A

132240372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717213-G-A

132240435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717270-G-A

132240528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138717367-A-G

132244007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719123-G-A

132244072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719188-A-G

132244209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719309-G-A

132244209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719309-G-C

132244254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719352-C-G

132244254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719352-C-T

132244324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719401-G-T

132244402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719479-G-T

132244473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719566-G-T

132244689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138719769-C-T

132245644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720558-G-A

http://identifiers.org/hco/10/GRCh38#132245678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138720626-C-A

132245732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720791-C-T

132245742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720843-G-A

http://identifiers.org/hco/10/GRCh38#132245749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138720850-C-A

132245749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720850-C-T

132245760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720861-A-G

132245842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720932-A-G

132245842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 138720932-A-T

http://identifiers.org/hco/10/GRCh38#132245857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138720951-C-A

132245857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138720951-C-T

132245985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138721076-G-A

132245985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 138721076-G-T

132252327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138724679-G-A

132252400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138724759-G-A

132252463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138724806-G-T

132252565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138724905-G-A

132255633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138726754-C-T

132255978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138727074-G-C

132255995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138727100-C-T

132256438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138727573-G-A

132256438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138727573-G-T

132257252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138728804-G-C

132258229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138729445-C-T

132258598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138729761-C-G

http://identifiers.org/hco/10/GRCh38#132258623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138729782-C-A

132258623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138729782-C-T

132258627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138729786-G-A

132258664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138729823-G-C

132258761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138729913-C-T

132258945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138730078-G-A

132258959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138730092-G-T

132265501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132265602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132265714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132265778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132266336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-C

132266349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/10/GRCh38#132266369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-A

http://identifiers.org/hco/10/GRCh38#132266460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-A

132266513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/10/GRCh38#132266629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-C

132266657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -T-C

132266703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132266721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132266874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/10/GRCh38#132266885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-C

http://identifiers.org/hco/10/GRCh38#132266899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-A

132266921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-C

132266921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-T

132266949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-G

132266949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132266985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132266985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-C

132266998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-C

132267050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-G

132267255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132267422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132267479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939641-G-A

132267481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939643-C-T

132267514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939670-T-C

132267526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939682-T-A

132267526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939682-T-G

132267530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939686-C-T

132267534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132267574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939708-C-T

132267588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 100939722-T-C

132269375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -T-C

132269409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132269540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132269695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-G

132269710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132269724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132269776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132269796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-G

132269894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/10/GRCh38#132269913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-A

132269913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-T

132269965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-T

http://identifiers.org/hco/10/GRCh38#132270146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -A-C

132270160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -G-A

132270228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -T-C

132270294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: -C-G

132274469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138739801-G-A

132274539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138739875-C-T

132274546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138739882-G-A

132274616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138739951-C-T

132274636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138739956-C-T

132274689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138739998-C-T

132275004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138740237-T-C

132275138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138740346-T-A

http://identifiers.org/hco/10/GRCh38#132275238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138740442-C-A

132275336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138740546-G-C

132277191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138741469-G-A

132277200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138741478-C-T

http://identifiers.org/hco/10/GRCh38#132277215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138741488-C-A

132277278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138741587-G-A

132277531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138741821-C-T

132277681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138741924-T-C

132277819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138741975-C-T

132278050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138742156-G-T

132278280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138742503-C-T

132281866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138744246-C-T

132281872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138744252-C-T

132282081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138744463-G-A

132289355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138747933-G-A

132289702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748265-G-C

132290073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748580-G-C

132290103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748609-C-T

132290439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748779-G-A

132290470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748811-A-G

132290501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748839-G-A

132290553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748892-C-T

132290575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748910-G-A

132290670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138748958-T-G

132290729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749017-C-T

132290819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749117-C-T

132290902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749176-A-G

132291004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749250-C-T

132291045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749273-T-C

132291150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749363-T-G

132291210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749421-G-A

132291283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749493-G-A

132291283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749493-G-C

132291637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749893-G-A

132291695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138749910-A-G

132291942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750001-G-C

132292025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750097-G-A

132292037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750109-T-C

132292118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750175-T-A

132292134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750191-A-G

132292399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750412-C-G

132292402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750415-T-A

132292584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138750511-T-C

132296820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138756721-G-A

132296830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138756731-G-A

132296860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138756764-A-G

132297011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138756910-G-A

http://identifiers.org/hco/10/GRCh38#132297287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138757142-A-C

132297308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757146-G-A

132297333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757165-G-A

132297426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757212-A-G

132297443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757221-C-G

132297443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757221-C-T

132297453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757231-T-A

132297456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757234-G-A

132297507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757274-G-C

132297509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138757276-T-A

132299692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138758815-C-T

132299745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138758868-T-C

132299808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138758927-C-T

132299809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138758928-G-A

132299815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138758934-C-T

132299916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138759006-C-T

132300316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138759421-A-G

132300374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138759480-G-A

132300474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138759577-C-G

132300474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138759577-C-T

132300503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138759606-G-C

132301946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761390-C-T

132301996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761435-G-T

132302017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761456-C-T

132302049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761474-G-A

132302129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761563-G-A

132302405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761838-G-A

132302428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761861-T-G

132302438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761871-C-T

132302456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761887-C-T

132302497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138761928-C-T

132304617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765153-G-A

132304640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765196-C-G

http://identifiers.org/hco/10/GRCh38#132304932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138765469-C-A

132304977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765510-T-C

132305025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765546-A-G

132305051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765567-G-A

132305108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765601-A-G

132305153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765635-G-A

132305153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765635-G-T

132305243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765651-A-G

http://identifiers.org/hco/10/GRCh38#132305412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138765822-C-A

132305582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138765982-C-G

132305700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138766097-C-T

132305860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138766239-G-T

132305888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138766267-G-A

132305934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138766327-G-A

http://identifiers.org/hco/10/GRCh38#132305939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138766349-C-A

132305939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138766349-C-T

132306068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138766464-C-T

132306810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767271-G-T

132306813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767274-C-T

http://identifiers.org/hco/10/GRCh38#132306830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138767286-C-A

http://identifiers.org/hco/10/GRCh38#132306883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138767330-C-A

132306883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767330-C-T

132306945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138767395-G-A

132306945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138767395-G-T

132307038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138767474-A-T

132307122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138767567-A-G

132307122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138767567-A-T

132307201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138767633-T-C

http://identifiers.org/hco/10/GRCh38#132307309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138767739-C-A

132307309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767739-C-G

132307309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767739-C-T

132307350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767777-G-A

132307350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767777-G-T

132307486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767894-G-A

132307486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767894-G-C

132307486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767894-G-T

http://identifiers.org/hco/10/GRCh38#132307493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138767901-C-A

http://identifiers.org/hco/10/GRCh38#132307496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138767910-C-A

132307496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767910-C-T

http://identifiers.org/hco/10/GRCh38#132307563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138767995-C-A

132307563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138767995-C-T

132307852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138768298-G-A

132307852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138768298-G-C

132307852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138768298-G-T

132307866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 138768312-T-C

132308024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768458-G-A

132308024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768458-G-T

132308094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768473-G-T

http://identifiers.org/hco/10/GRCh38#132308124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138768483-C-A

132308124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768483-C-G

132308124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768483-C-T

132308131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768490-G-T

132308149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768513-G-A

http://identifiers.org/hco/10/GRCh38#132308160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138768525-A-C

132308165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768530-G-C

http://identifiers.org/hco/10/GRCh38#132308178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138768537-A-C

132308206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768560-G-C

http://identifiers.org/hco/10/GRCh38#132308213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138768567-C-A

132308325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138768673-T-G

http://identifiers.org/hco/10/GRCh38#132309156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#138770329-C-A

132309204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron variant
orthologous variants: 138770378-C-T

132332077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, undefined
orthologous variants: 138793097-G-T

132332084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, undefined
orthologous variants: 138793104-C-T

132332093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: intron_variant, undefined
orthologous variants: 138793113-C-T

132332179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 138793188-G-A

132332179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21332
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 138793188-G-T