128300114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29115810-C-T

128300131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29115826-G-T

128300132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29115827-G-T

128300145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29115840-A-G

http://identifiers.org/hco/7/GRCh38#128300153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29115848-C-A

128300213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29115896-A-G

128300259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29115910-G-T

http://identifiers.org/hco/7/GRCh38#128300314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29115971-C-A

128300553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116097-A-G

128300569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116113-G-A

128300599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116150-G-A

128300599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116150-G-T

128300625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116173-T-C

128300737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116287-G-A

128300741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116291-G-A

128300741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116291-G-T

128301013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116426-A-G

http://identifiers.org/hco/7/GRCh38#128301020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29116433-C-A

128301020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116433-C-T

128301059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116455-T-A

128301156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116524-C-T

128301355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116736-A-G

http://identifiers.org/hco/7/GRCh38#128301386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29116757-C-A

128301467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116818-C-T

128301475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116826-G-A

http://identifiers.org/hco/7/GRCh38#128301493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29116843-C-A

128301493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116843-C-T

http://identifiers.org/hco/7/GRCh38#128301497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29116847-C-A

128301497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116847-C-T

http://identifiers.org/hco/7/GRCh38#128301498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29116848-C-A

128301498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116848-C-T

128301594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29116933-C-T

http://identifiers.org/hco/7/GRCh38#128301602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29116941-C-A

128301822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29117210-G-C

128301905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29117279-A-G

128301905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29117279-A-T

128302001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29117361-A-G

128302403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29117754-A-G

http://identifiers.org/hco/7/GRCh38#128302535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29117888-C-A

128302676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118048-A-G

http://identifiers.org/hco/7/GRCh38#128302846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29118279-C-A

128303079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118441-G-A

128303079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118441-G-T

128303093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118456-A-G

128303285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118600-G-T

128303337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118629-A-T

128303361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118653-C-T

128303394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118680-T-A

128303394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118680-T-C

128303588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118830-G-T

128303720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29118921-T-A

128303830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119015-T-A

http://identifiers.org/hco/7/GRCh38#128303841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29119026-C-A

http://identifiers.org/hco/7/GRCh38#128303847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29119032-A-C

128303878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119063-G-T

128303903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119086-G-C

128303903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119086-G-T

http://identifiers.org/hco/7/GRCh38#128303917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29119100-C-A

128303922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119101-G-C

128303922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119101-G-T

128303925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119104-A-G

128303935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119114-T-C

128303955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119194-G-A

128303960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119199-T-C

128303973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119230-G-A

128304014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119270-T-C

128304106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119460-G-T

128304380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119755-C-T

128304400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119774-G-T

128304533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119883-T-C

128304548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119898-A-T

128304557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29119904-C-G

128305256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120151-T-C

128305298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120189-A-G

128305363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120235-G-T

http://identifiers.org/hco/7/GRCh38#128305438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29120303-C-A

128305706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120388-G-T

128305768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120445-G-A

128305768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120445-G-T

128305783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120459-A-G

128305792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120468-C-T

128305827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120503-G-A

128305827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120503-G-T

128305835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120511-G-T

128305851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120512-T-A

128305851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120512-T-C

128305859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120520-A-G

128305883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120544-G-T

128305941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120649-G-T

128305999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120700-C-T

128306075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120734-G-T

128306167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120821-G-A

128306167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120821-G-T

http://identifiers.org/hco/7/GRCh38#128306203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29120832-C-A

http://identifiers.org/hco/7/GRCh38#128306247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29120875-C-A

128306247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120875-C-T

128306318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29120936-G-T

128306397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29121021-C-T

128306415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29121039-G-A

128306415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29121039-G-T

http://identifiers.org/hco/7/GRCh38#128306416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29121040-C-A

128306416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29121040-C-T

http://identifiers.org/hco/7/GRCh38#128306690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29121439-C-A

http://identifiers.org/hco/7/GRCh38#128306699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29121448-C-A

128306699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121448-C-T

http://identifiers.org/hco/7/GRCh38#128306716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29121464-A-C

128306716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121464-A-G

128306769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121518-G-A

128306769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121518-G-T

128306790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121539-A-G

128306827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121581-A-G

128306919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121697-A-T

128306983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121748-A-G

http://identifiers.org/hco/7/GRCh38#128306984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29121749-C-A

128307012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121771-G-T

128307038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121797-T-C

128307072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121831-A-G

128307093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121854-A-G

http://identifiers.org/hco/7/GRCh38#128307117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29121874-C-A

128307143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121903-T-C

128307145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121905-A-G

128307163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29121923-T-C

128307292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29122055-G-A

128307292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29122055-G-T

128307388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29122164-G-A

128307713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29122798-T-C

128307985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29122935-A-G

128308421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123348-A-G

128308434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123361-G-T

128308455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123384-T-C

http://identifiers.org/hco/7/GRCh38#128308584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29123496-C-A

http://identifiers.org/hco/7/GRCh38#128308597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29123511-C-A

128308747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123666-A-G

128308841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123765-G-C

128308841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123765-G-T

http://identifiers.org/hco/7/GRCh38#128308900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29123841-C-A

128308953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29123959-G-T

128309075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124092-T-C

128309143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124160-T-C

128309666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124291-G-T

http://identifiers.org/hco/7/GRCh38#128309767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29124386-C-A

128309805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124420-A-G

128309812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124427-G-A

128309812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124427-G-C

128309836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124450-G-T

http://identifiers.org/hco/7/GRCh38#128310181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29124853-C-A

http://identifiers.org/hco/7/GRCh38#128310245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29124918-C-A

128310245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124918-C-G

128310245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124918-C-T

128310313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124978-C-T

128310335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29124992-G-T

http://identifiers.org/hco/7/GRCh38#128310340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29124997-A-C

128310376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29125029-T-A

128310376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29125029-T-C

128310376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3 prime UTR variant
orthologous variants: 29125029-T-G

128310529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125198-A-T

http://identifiers.org/hco/7/GRCh38#128310665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29125308-C-A

128310665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125308-C-T

128310684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125325-A-T

128310712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125352-G-A

128310712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125352-G-C

128310712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125352-G-T

128310713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29125353-T-G

128310923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29125515-C-G

128311344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125971-G-A

128311385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126009-T-C

128311760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126664-G-A

128311760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126664-G-C

128311771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29126675-T-A

128312476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127141-G-A

128312482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127147-G-A

128312501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127166-T-C

128312512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127172-A-G

128312512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127172-A-T

128312513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127173-G-A

128312550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127214-C-T

128312729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127390-A-G

128312800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127453-T-A

128312942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127613-G-T

128312979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127656-G-A

128312979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29127656-G-C

http://identifiers.org/hco/7/GRCh38#128313038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29127688-C-A

128313140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29127761-T-C

128313163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29127785-T-G

128313357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128008-C-G

128314407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128163-T-C

128314612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128313-G-T

http://identifiers.org/hco/7/GRCh38#128314643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29128341-A-C

128314661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128357-C-G

128314671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128367-C-T

http://identifiers.org/hco/7/GRCh38#128314672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29128368-A-C

128314672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128368-A-T

http://identifiers.org/hco/7/GRCh38#128314674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29128370-A-C

128314674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128370-A-G

128314675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128371-C-G

128314675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128371-C-T

128314716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128411-G-A

128314716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128411-G-C

128314780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 29128444-G-A

128315134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128796-C-G

128315134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29128796-C-T

128315427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29129064-C-T

128315459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29129101-C-T

128315679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29129265-G-C

128316827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130285-C-T

128316843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130301-T-C

128316875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130326-G-A

128316954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130386-T-G

http://identifiers.org/hco/7/GRCh38#128317117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29130536-A-C

128317353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130743-T-C

128317467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130852-G-A

128317506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130891-T-C

128317534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130918-G-A

128317534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130918-G-T

128317595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131102-G-C

128317595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131102-G-T

128317716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29131323-G-A

128317716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29131323-G-C

128317753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131356-T-C

http://identifiers.org/hco/7/GRCh38#128317813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29131450-A-C

http://identifiers.org/hco/7/GRCh38#128317815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29131452-C-A

128317815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131452-C-G

128317864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131573-C-G

128317877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131585-G-T

128318053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29131722-G-A

128318098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 29131767-C-T

128318753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132558-T-A

128318811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132614-T-C

128318935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132724-C-T

128319040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132807-A-G

128319062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132833-G-A

128319062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132833-G-T

128319160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29132935-T-C

http://identifiers.org/hco/7/GRCh38#128319624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29133812-C-A

128319713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29133892-C-G

128320696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134871-T-A

128320730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134905-G-A

128320958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29135068-G-C

http://identifiers.org/hco/7/GRCh38#128321166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29135302-A-C

http://identifiers.org/hco/7/GRCh38#128321170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29135306-C-A

http://identifiers.org/hco/7/GRCh38#128321174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29135310-C-A

128321212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29135371-G-A

128321212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29135371-G-T

128321240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29135384-C-T

128321263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29135404-C-T

http://identifiers.org/hco/7/GRCh38#128321276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29135417-C-A

128321276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29135417-C-T

128321291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29135432-C-G

128321356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29135497-C-T

128321523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29135664-C-T

http://identifiers.org/hco/7/GRCh38#128321574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29135699-C-A

128321831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29135964-C-T

128321912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29136062-G-C

128322103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29136289-T-C

128322130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29136316-C-T

128323429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29137485-T-C

128323501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29137552-T-C

128323662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29137713-T-C

http://identifiers.org/hco/7/GRCh38#128323879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29137901-C-A

http://identifiers.org/hco/7/GRCh38#128324416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29138370-A-C

128324416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138370-A-G

128324416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138370-A-T

128324451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138406-C-G

128324503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138443-A-G

128324504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138444-T-C

128324505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138445-G-A

128324505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138445-G-C

128324670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29138613-G-A

128324670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 29138613-G-C

128324690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, missense_variant, stop_gained
orthologous variants: 29138633-C-T

128325097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29138854-C-T

128325490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139078-C-T

128325547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139136-C-T

128325654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139398-T-C

http://identifiers.org/hco/7/GRCh38#128325683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29139431-A-C

128325786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139515-G-A

128325786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139515-G-T

128325903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139637-G-T

128326021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139770-G-A

128326059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139808-C-G

http://identifiers.org/hco/7/GRCh38#128327257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29139922-C-A

128327333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29139993-C-T

128329520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29142575-C-T

128329909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29142989-A-G

http://identifiers.org/hco/7/GRCh38#128329954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29143027-A-C

128329980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143053-G-C

128330295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143369-T-G

128330684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143452-T-C

128330684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143452-T-G

128330719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143486-G-A

128330719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143486-G-T

128330781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143520-T-C

128330871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 29143605-T-G

128330901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 29143635-T-C

http://identifiers.org/hco/7/GRCh38#128330955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29143686-A-C

128331130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143900-G-A

128331147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29143917-A-G

128331352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29144120-T-C

128331528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29144314-A-G

128331678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29144459-A-G

128331678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29144459-A-T

128333156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152108-G-A

128333156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152108-G-T

128333266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152234-A-T

128333277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152268-C-G

128333283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29152274-G-A

128333283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 29152274-G-T

128333314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29152305-T-C

128333314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29152305-T-G

128333694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152593-G-A

128333847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152667-T-C

128334031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29152794-A-G

128334190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29153014-A-G

128334191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29153015-T-C

128334244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29153105-G-A

128334273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29153132-G-T

128334285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29153144-C-G

128334880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29153672-G-A

128335518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29154728-G-A

128335688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29154901-G-C

128335726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29154939-C-T

128336076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29155218-T-C

128336573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29156529-G-A

128336577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29156533-G-A

http://identifiers.org/hco/7/GRCh38#128337082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29157014-C-A

128337089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29157021-G-T

128337108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29157039-C-T

http://identifiers.org/hco/7/GRCh38#128337117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29157053-C-A

128337120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29157056-C-T

128337220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29157156-G-A

http://identifiers.org/hco/7/GRCh38#128337318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29157243-A-C

128337318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29157243-A-T

http://identifiers.org/hco/7/GRCh38#128337553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29157454-C-A

128337912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29157730-G-A

128337912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29157730-G-C

http://identifiers.org/hco/7/GRCh38#128338126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29158044-C-A

128338126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158044-C-T

http://identifiers.org/hco/7/GRCh38#128338209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29158129-C-A

128338473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158384-G-A

128338473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158384-G-T

128338577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158474-A-G

128338585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158482-T-C

128338601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158498-A-G

128338861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29158979-C-T

128338938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159063-G-A

128338938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159063-G-T

http://identifiers.org/hco/7/GRCh38#128339083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29159529-C-A

128339083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159529-C-T

128339103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159547-T-G

128339146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159582-T-C

128339171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159605-C-T

128339316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant
orthologous variants: 29159744-A-G

128339331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159759-A-G

http://identifiers.org/hco/7/GRCh38#128339389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29159806-A-C

128339405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159821-G-A

128339405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159821-G-T

128339446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159852-C-T

128339508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159923-G-A

128339508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159923-G-T

128339565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159984-C-G

128339565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159984-C-T

128339574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29159993-T-G

128339599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29160015-G-A

128339697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29160100-G-A

http://identifiers.org/hco/7/GRCh38#128340087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29160455-C-A

128340122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29160493-A-G

http://identifiers.org/hco/7/GRCh38#128340129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29160500-C-A

128340129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29160500-C-G

128341114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29161600-T-G

128341125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29161611-G-A

128341125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 29161611-G-T

128341147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant
orthologous variants: 29161627-G-A

128341147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant
orthologous variants: 29161627-G-C

128341148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant
orthologous variants: 29161628-C-T

128341165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant
orthologous variants: 29161645-T-C

128341165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, missense_variant
orthologous variants: 29161645-T-G

http://identifiers.org/hco/7/GRCh38#128341175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#29161655-C-A

128341296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162485-G-T

128341330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162534-G-C

128341330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162534-G-T

128341331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162535-A-G

128341348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162551-T-A

128341348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162551-T-C

128341445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162629-C-T

128341501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162655-A-G

128341536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162677-T-C

128341594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162737-G-A

128341608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29162752-T-C

128343212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29163743-T-C

http://identifiers.org/hco/7/GRCh38#128343387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29163917-C-A

128343387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29163917-C-T

128343420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29163948-T-C

128343531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29164225-A-G

128343543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: intron variant
orthologous variants: 29164237-G-T

128343826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: 29164637-G-A

128343826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: 29164637-G-T

http://identifiers.org/hco/7/GRCh38#128343833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29164644-C-A

128343833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: 29164644-C-G

128343833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: 29164644-C-T

http://identifiers.org/hco/7/GRCh38#128343885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29164696-C-A

128343885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21863
most severe consequence: 5 prime UTR variant
orthologous variants: 29164696-C-T