129001402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707675-G-A

129001476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707745-C-G

129001476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707745-C-T

129001484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707753-G-A

129001484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707753-G-C

129001503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707771-G-A

129001503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707771-G-C

129001503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707771-G-T

129001519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707787-G-T

129001520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707788-A-G

http://identifiers.org/hco/3/GRCh38#129001522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707790-C-A

129001522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707790-C-T

129001578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707830-G-A

129001578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707830-G-T

http://identifiers.org/hco/3/GRCh38#129001584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707836-A-C

129001584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707836-A-T

http://identifiers.org/hco/3/GRCh38#129001601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707845-C-A

129001601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707845-C-T

129001653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707864-G-A

129001653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 87707864-G-T

http://identifiers.org/hco/3/GRCh38#129001654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87707865-A-C

129001654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707865-A-G

129001655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87707866-G-A

129001655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707866-G-C

129001655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87707866-G-T

http://identifiers.org/hco/3/GRCh38#129001854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708067-C-A

129001854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708067-C-G

129001854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708067-C-T

129001877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708090-C-T

http://identifiers.org/hco/3/GRCh38#129001884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708097-C-A

129001884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708097-C-T

http://identifiers.org/hco/3/GRCh38#129001927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708128-C-A

129001927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708128-C-G

129001927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708128-C-T

129001935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708136-G-A

129001952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708153-G-C

129001960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708161-G-A

129001960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708161-G-C

129001960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708161-G-T

129001975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708176-A-G

129001984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708185-C-T

http://identifiers.org/hco/3/GRCh38#129002037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708238-C-A

129002037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708238-C-G

129002037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708238-C-T

http://identifiers.org/hco/3/GRCh38#129002129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708330-C-A

129002129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708330-C-G

129002129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87708330-C-T

http://identifiers.org/hco/3/GRCh38#129002138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708339-C-A

129002138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708339-C-G

http://identifiers.org/hco/3/GRCh38#129002150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708351-C-A

http://identifiers.org/hco/3/GRCh38#129002177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708378-C-A

129002177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87708378-C-T

129002205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708403-A-G

129002205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708403-A-T

http://identifiers.org/hco/3/GRCh38#129002225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708423-C-A

129002225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87708423-C-G

129002225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87708423-C-T

129002267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708465-G-T

http://identifiers.org/hco/3/GRCh38#129002309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708507-C-A

129002369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708535-G-A

129002369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708535-G-C

129002369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708535-G-T

129002371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708537-T-C

129002425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708543-G-A

129002425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708543-G-C

129002428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708546-G-A

129002488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708604-T-C

http://identifiers.org/hco/3/GRCh38#129002510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708625-C-A

129002510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87708625-C-T

http://identifiers.org/hco/3/GRCh38#129002620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87708680-A-C

129002620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708680-A-G

129002644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87708703-T-A

129002702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708740-G-T

129002713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708751-G-A

129002713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87708751-G-T

129003152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709066-A-G

129003365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709318-A-G

129003436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709406-G-C

129003436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709406-G-T

http://identifiers.org/hco/3/GRCh38#129003438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87709408-A-C

129003494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709451-G-A

129003494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709451-G-T

129003566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709523-T-G

129003699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709593-G-A

129003699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87709593-G-T

129003718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709612-G-A

129003718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709612-G-C

129003718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709612-G-T

http://identifiers.org/hco/3/GRCh38#129003887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87709728-C-A

129003887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87709728-C-G

129003887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709728-C-T

129003940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709781-G-A

129003940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87709781-G-T

129003963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87709804-G-A

129003963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87709804-G-C

129003963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87709804-G-T

129003973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87709814-G-A

129003973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87709814-G-T

129004021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87709862-G-A

129004021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87709862-G-T

http://identifiers.org/hco/3/GRCh38#129004097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87709956-C-A

129004097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709956-C-T

http://identifiers.org/hco/3/GRCh38#129004102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87709961-C-A

129004102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709961-C-T

129004123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87709977-C-G

http://identifiers.org/hco/3/GRCh38#129004150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87710003-A-C

129004150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87710003-A-G

http://identifiers.org/hco/3/GRCh38#129004153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#87710006-C-A

129004209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710047-T-C

129004649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710196-G-A

129004649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710196-G-T

129004814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710349-C-T

129004936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710468-G-A

http://identifiers.org/hco/3/GRCh38#129004957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87710487-C-A

129005232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710709-A-T

129005436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87710898-C-T

129005656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87711148-G-T

129005865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87711342-T-C

129005972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87711422-C-T

129006051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87711499-A-G

129008133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87713975-G-C

129008327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87714125-C-T

129008435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87714217-C-T

129008588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87714340-G-A

129008639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87714393-A-T

129009810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87714804-C-T

129010061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715020-G-A

129010061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715020-G-T

129010171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715107-C-T

129010433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715265-A-G

129010484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715321-G-A

129010883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715603-C-T

129011075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715793-G-A

129011080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715798-G-C

129011097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715814-G-A

129011101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87715818-C-G

129014583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87715991-G-A

129014779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716126-C-G

129014779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716126-C-T

129014807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716148-C-T

129014926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716245-C-G

129015097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716404-G-A

129015130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716436-C-T

129015172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716477-A-T

129015304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716588-A-G

129015304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716588-A-T

129015341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716617-T-C

129015506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716759-G-A

129015730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716871-C-T

129015830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87716961-T-G

129015997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87717104-G-C

129016501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87717415-C-G

129016501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87717415-C-T

http://identifiers.org/hco/3/GRCh38#129016513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87717427-C-A

http://identifiers.org/hco/3/GRCh38#129016550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87717442-C-A

129016550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87717442-C-T

129016742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87717606-G-A

129016802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87717665-G-A

129016838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87717701-C-G

129022329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87723869-C-T

129022509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724016-C-T

129022516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724023-G-T

129022521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724028-C-T

129022758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724231-T-C

129025815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724448-C-T

129025861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724497-C-T

129025922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87724557-C-T

129030518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87725940-A-G

129030534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87725956-T-C

129030534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87725956-T-G

129030552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87725972-T-C

129030556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87725973-A-G

129030557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87725974-G-A

http://identifiers.org/hco/3/GRCh38#129030587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87726003-A-C

129030597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87726013-G-T

129030619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87726034-A-T

129030626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87726041-G-A

129030626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87726041-G-T

129030684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87726097-G-A

129030714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87726125-C-T

129030727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87726138-C-T

129030732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87726143-A-G

129030867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87726266-C-G

http://identifiers.org/hco/3/GRCh38#129030947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87726342-C-A

129031626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87726839-T-C

129031669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87726876-C-T

129031966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727119-G-C

129032266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727361-C-G

129032809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727593-G-C

129032809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727593-G-T

129032912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87727689-C-T

129032928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87727706-C-G

129032928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87727706-C-T

129033004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727765-A-G

129033006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727767-G-A

129033006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727767-G-T

129033034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727785-G-A

129033034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727785-G-T

129033044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727795-G-A

129033044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87727795-G-T

129033498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728238-G-A

129033912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728551-A-G

129033932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728569-A-T

129034035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728658-G-A

129034035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728658-G-T

129034047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728670-C-T

129034048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728671-G-A

129034048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728671-G-T

129034379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728918-C-T

129034394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728933-G-T

http://identifiers.org/hco/3/GRCh38#129034419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87728945-C-A

129034419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87728945-C-G

129034495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87729015-G-A

129036841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87729840-G-A

129036841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87729840-G-T

129036861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87729859-A-T

129036887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87729899-C-G

129036953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87730008-G-A

129036957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87730012-T-C

129036985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87730038-G-T

129037006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87730056-T-C

129037009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87730059-G-A

129037021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87730071-G-A

129037053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87730103-G-A

129038730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87730622-C-T

http://identifiers.org/hco/3/GRCh38#129038788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87730680-C-A

129038788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87730680-C-G

129038788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87730680-C-T

http://identifiers.org/hco/3/GRCh38#129038892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87730778-C-A

http://identifiers.org/hco/3/GRCh38#129039145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87731078-A-C

129039190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731119-C-T

129039238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731166-A-G

129039358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731253-A-G

129039448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731391-C-T

129039611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731613-A-G

129039633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731632-T-C

129039636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731635-G-T

129039666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731661-G-A

129039666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87731661-G-C

http://identifiers.org/hco/3/GRCh38#129039726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87731719-C-A

129039744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87731737-G-A

129039794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87731787-G-A

129039794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87731787-G-C

129039794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87731787-G-T

http://identifiers.org/hco/3/GRCh38#129039830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87731823-C-A

129039830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87731823-C-T

129039853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87731846-A-G

129039890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87731883-G-A

129039890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87731883-G-T

129039908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87731925-A-G

http://identifiers.org/hco/3/GRCh38#129039913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87731930-C-A

129039913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87731930-C-T

http://identifiers.org/hco/3/GRCh38#129039916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87731933-C-A

129039916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87731933-C-T

http://identifiers.org/hco/3/GRCh38#129039921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87731938-C-A

129039990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732095-A-G

http://identifiers.org/hco/3/GRCh38#129040019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732122-C-A

129040019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732122-C-T

http://identifiers.org/hco/3/GRCh38#129040045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732148-C-A

129040045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732148-C-T

129040104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732185-T-A

129040104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732185-T-C

129040104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732185-T-G

129040105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732186-G-A

129040105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732186-G-T

129040111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732192-G-A

129040111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732192-G-T

129040116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732197-A-T

129040157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732238-G-T

129040161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732242-G-T

http://identifiers.org/hco/3/GRCh38#129040204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732265-C-A

129040204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732265-C-T

http://identifiers.org/hco/3/GRCh38#129040205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732266-C-A

129040205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732266-C-T

129040215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732276-G-T

http://identifiers.org/hco/3/GRCh38#129040269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732329-A-C

129040269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732329-A-G

http://identifiers.org/hco/3/GRCh38#129040277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732337-C-A

129040277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732337-C-T

http://identifiers.org/hco/3/GRCh38#129040288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732348-C-A

http://identifiers.org/hco/3/GRCh38#129040315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732376-C-A

129040315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732376-C-G

129040315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732376-C-T

129040423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732482-G-A

129040435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732494-G-A

129040435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732494-G-C

129040441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732500-G-T

http://identifiers.org/hco/3/GRCh38#129040448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732507-A-C

129040448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732507-A-G

129040481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732521-A-G

129040521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732568-G-A

129040521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732568-G-T

http://identifiers.org/hco/3/GRCh38#129040532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#87732578-C-A

129040532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25692
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87732578-C-T