135906728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 3 prime UTR variant
orthologous variants: 128291490-T-C

http://identifiers.org/hco/2/GRCh38#135906872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128291598-A-C

135906939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128291659-C-T

135906976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128291697-G-T

135907221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128291949-G-A

135907221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 128291949-G-T

135907322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128291977-A-G

135907367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128292022-A-G

135907373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128292028-C-T

135907434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128292088-T-C

135911079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128294378-T-C

135911143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128294439-G-A

135911143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128294439-G-C

135911143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128294439-G-T

135911278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294551-T-C

135911278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294551-T-G

135911288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294572-T-A

135911288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294572-T-C

135911310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294588-G-A

135911310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294588-G-T

http://identifiers.org/hco/2/GRCh38#135911497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128294773-C-A

135911497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128294773-C-G

135911497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128294773-C-T

135911581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128294856-G-A

135911581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128294856-G-C

135911581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128294856-G-T

135911623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294890-T-A

135911623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294890-T-C

135911654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294916-A-T

135911655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294917-T-A

135911655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294917-T-C

http://identifiers.org/hco/2/GRCh38#135911697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128294956-A-C

135911747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128294996-T-C

135911759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128295006-T-A

135911759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128295006-T-C

135911780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128295027-G-A

135912147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128295632-A-G

http://identifiers.org/hco/2/GRCh38#135912474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128296090-C-A

135912474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296090-C-T

135912486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 128296102-G-A

135912486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 128296102-G-T

135912543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128296159-A-G

135913250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296289-G-T

135913891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296587-T-C

135913894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296591-T-C

135913894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296591-T-G

135914144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296768-G-C

135914233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296841-A-G

135914302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296899-T-G

135914306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128296903-T-C

135914355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297116-T-C

135914357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297118-T-C

135914357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297118-T-G

135914360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297121-A-G

135914360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297121-A-T

135914372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297133-T-C

135914381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297142-A-G

135914381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128297142-A-T

http://identifiers.org/hco/2/GRCh38#135914542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128297303-A-C

135914542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128297303-A-G

135915880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128299692-G-T

135916220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128299871-A-G

135916220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128299871-A-T

135916285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128299936-A-G

135916611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128300237-G-A

135916615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128300241-A-G

135918447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301313-C-T

http://identifiers.org/hco/2/GRCh38#135920411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128301632-A-C

135920433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301654-G-C

135920439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301660-A-G

135920442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301663-A-G

135920557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128301778-C-T

135920650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301867-G-A

135920651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301868-A-G

135920688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301905-G-T

135920721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128301940-T-C

135920825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128302035-A-G

135921259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128302338-T-G

135921425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128302494-G-A

135921717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128302910-A-G

135921750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128302939-C-T

135921889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128303050-A-G

http://identifiers.org/hco/2/GRCh38#135922601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128303690-C-A

135922601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128303690-C-T

135922648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128303774-T-C

135922652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128303778-A-G

135922750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128303850-T-C

135922839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128303970-T-C

135922887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128304018-A-G

135922925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 128304056-G-A

135922925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 128304056-G-C

135922925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 128304056-G-T

135922942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128304067-A-G

135922942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128304067-A-T

135922945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128304070-T-C

135922948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128304073-T-C

135922948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128304073-T-G

135922949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128304074-T-C

135923845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306128-C-T

135923910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306176-G-A

135924108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306268-T-A

135924284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306410-A-G

http://identifiers.org/hco/2/GRCh38#135924415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128306531-C-A

135924507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306623-C-T

135924509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306625-G-A

135924612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306715-T-C

http://identifiers.org/hco/2/GRCh38#135924613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128306716-C-A

135924613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306716-C-G

135924624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306727-A-G

135924650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306750-T-A

135924650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306750-T-C

135924650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128306750-T-G

135925052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128307154-T-C

135925056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128307158-T-A

135925056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128307158-T-C

http://identifiers.org/hco/2/GRCh38#135925106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128307210-A-C

135925181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128307286-T-A

135925550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128307800-G-A

135925865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128308196-T-C

135925895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128308230-T-C

135926510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128308804-C-T

135926663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309003-T-C

135926663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309003-T-G

135926702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309041-C-T

135926787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309125-C-T

135926943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309251-C-T

http://identifiers.org/hco/2/GRCh38#135926958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128309266-C-A

135928141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309895-T-C

135928205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128309972-C-T

135928296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128310045-A-T

135928373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128310431-A-T

http://identifiers.org/hco/2/GRCh38#135929111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128310635-A-C

135929355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128310846-G-A

135929355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128310846-G-C

http://identifiers.org/hco/2/GRCh38#135929387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128310874-C-A

135929478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128310958-G-A

135931856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314040-C-T

135932308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128314457-C-T

135932513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314617-C-T

135932551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314655-G-C

http://identifiers.org/hco/2/GRCh38#135932604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128314704-C-A

135932660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314751-T-C

135932660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314751-T-G

135932689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314780-A-G

135932689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314780-A-T

135932733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314807-C-T

135932748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314822-A-G

135932773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314844-T-A

135932773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128314844-T-C

135932801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128314872-G-A

135932801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: missense variant
orthologous variants: 128314872-G-T

http://identifiers.org/hco/2/GRCh38#135932828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128314899-A-C

135932828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128314899-A-G

135932828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: synonymous variant
orthologous variants: 128314899-A-T

http://identifiers.org/hco/2/GRCh38#135932861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128314932-A-C

135932861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128314932-A-G

135932861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128314932-A-T

135932873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128314973-T-A

135932873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128314973-T-C

135932873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128314973-T-G

135932922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128315032-T-C

135933006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128315119-G-A

135933798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128316766-T-C

135933798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128316766-T-G

135934087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317016-G-A

135934726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317439-T-C

135935211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317555-G-A

135935281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317618-G-A

135935281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317618-G-C

135935857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317828-G-A

135935947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128317894-C-T

135936132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318051-T-A

135936132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318051-T-C

135936167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318082-G-A

135936753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318393-T-C

135936753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318393-T-G

135936758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318398-A-G

135936764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318404-G-A

135936764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron variant
orthologous variants: 128318404-G-C

135943583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128319211-T-A

135943583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128319211-T-C

135943594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128319222-A-G

http://identifiers.org/hco/2/GRCh38#135944356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128319694-C-A

135944539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128319841-C-T

135944651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128319956-C-G

135946432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128323384-T-C

135946570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128323566-A-G

135946615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128323604-G-A

http://identifiers.org/hco/2/GRCh38#135947958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128325688-C-A

135947958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128325688-C-T

135948908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128326895-T-A

135949211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128327299-C-T

135949350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128327467-A-G

135950785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128328813-T-C

135950806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128328825-T-C

135950883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128328899-T-C

http://identifiers.org/hco/2/GRCh38#135951740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128329193-A-C

135951978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128329437-T-C

135952015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128329474-T-G

135953315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128329863-T-C

135953334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128329881-C-G

135953447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128329975-G-C

135953596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128330114-G-A

135953634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128330153-G-A

135953789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128330308-G-A

135958647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128330623-C-G

135958901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128330868-T-C

135958964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128330953-T-C

135958996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128331048-A-G

135959183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128331191-G-C

135959901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128331829-T-C

135959947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128331894-T-C

135960690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128332423-A-G

135960896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128332611-C-T

135960916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128332630-C-T

135961401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128333108-A-G

135962162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128333810-C-T

135962210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128333856-T-C

135962295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128333919-G-A

135962311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128333938-C-T

http://identifiers.org/hco/2/GRCh38#135962542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128334155-C-A

135962647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128334399-T-C

135962949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128334686-T-A

135963069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128334801-T-C

135963079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128334811-T-C

135963219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128335082-G-A

http://identifiers.org/hco/2/GRCh38#135963264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128335128-A-C

135964086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128335697-C-T

135964158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128335754-C-G

135966019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128339097-G-T

135979323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128341446-A-G

135979323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128341446-A-T

135979341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128341464-G-A

135979341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128341464-G-C

135979341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128341464-G-T

135979847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128341924-G-A

http://identifiers.org/hco/2/GRCh38#135979890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128341958-C-A

135979989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128342052-C-T

135980488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128342274-G-T

135980543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128342324-A-G

135980678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128342421-A-G

135983247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343011-G-A

135983247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343011-G-T

http://identifiers.org/hco/2/GRCh38#135983322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128343044-A-C

135983322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343044-A-T

135983401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128343095-T-A

135983401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128343095-T-C

135983401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128343095-T-G

135983465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343161-A-G

135983465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343161-A-T

135983527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343205-T-C

135983691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343364-T-C

135983882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128343557-C-T

135984268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128343910-T-C

135984388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128344029-C-T

135984693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128344235-T-C

135984962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128344447-T-G

135985027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128344506-G-A

135985053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128344531-A-G

135985116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128344598-G-A

http://identifiers.org/hco/2/GRCh38#135985120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128344602-C-A

http://identifiers.org/hco/2/GRCh38#135985244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128344734-C-A

135985312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128344810-A-G

135985312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128344810-A-T

135985459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 128344945-C-T

http://identifiers.org/hco/2/GRCh38#135985492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#128344979-A-C

135985492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 128344979-A-G

http://identifiers.org/hco/2/GRCh38#135985515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128345002-C-A

135985515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 128345002-C-G

135985606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128345084-G-T

135985619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128345097-A-G

135985636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345114-T-C

135985668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345132-G-A

http://identifiers.org/hco/2/GRCh38#135985689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128345150-C-A

135985689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345150-C-T

http://identifiers.org/hco/2/GRCh38#135985697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128345155-C-A

135985697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345155-C-T

http://identifiers.org/hco/2/GRCh38#135985737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128345182-C-A

135985737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345182-C-T

http://identifiers.org/hco/2/GRCh38#135985744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128345189-A-C

135985744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345189-A-G

135985772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345217-T-C

135985834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345264-T-C

135985842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128345272-G-T

http://identifiers.org/hco/2/GRCh38#135985861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#128345297-C-A

135985861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128345297-C-T

135986026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128345613-C-T

135986071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128345668-G-A

135986071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128345668-G-C

135986071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2678
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128345668-G-T