142592225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38971770-G-A

142592260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38971802-A-G

142592288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38971832-T-C

142592322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38971873-G-T

http://identifiers.org/hco/5/GRCh38#142592483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38972004-A-C

142592523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972044-T-C

http://identifiers.org/hco/5/GRCh38#142592537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38972078-C-A

http://identifiers.org/hco/5/GRCh38#142592549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38972090-C-A

142592679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972204-A-G

142592713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972252-G-A

142592713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972252-G-T

142592784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972322-G-T

142592787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972325-A-G

http://identifiers.org/hco/5/GRCh38#142592818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38972349-C-A

142592870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972396-G-T

142592996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972512-G-T

142593036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972551-G-A

142593036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972551-G-T

142593041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972556-A-G

142593094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972603-G-C

142593094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972603-G-T

http://identifiers.org/hco/5/GRCh38#142593278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38972786-C-A

142593305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38972810-G-T

142593530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38973190-T-C

142593566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38973224-C-T

142593924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38973695-T-C

142593925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38973696-G-T

142593984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38973759-T-C

http://identifiers.org/hco/5/GRCh38#142594240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38973976-C-A

142594240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38973976-C-T

http://identifiers.org/hco/5/GRCh38#142594372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974105-C-A

142594387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974121-A-G

142594408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974145-G-A

142594408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974145-G-T

http://identifiers.org/hco/5/GRCh38#142594466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974208-C-A

http://identifiers.org/hco/5/GRCh38#142594468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974210-C-A

142594468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974210-C-T

http://identifiers.org/hco/5/GRCh38#142594490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974230-C-A

142594681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974386-C-T

142594706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974406-G-A

142594706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974406-G-T

142594738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974438-A-G

142594768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974470-T-C

http://identifiers.org/hco/5/GRCh38#142594796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974505-C-A

142594861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974554-G-A

142594861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974554-G-T

142595122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974839-A-G

142595153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974871-G-A

142595153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38974871-G-T

http://identifiers.org/hco/5/GRCh38#142595168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974884-C-A

http://identifiers.org/hco/5/GRCh38#142595200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38974916-C-A

142595200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38974916-C-T

142595268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38974958-T-G

142595305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38974995-T-A

142595305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38974995-T-C

142595356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38975046-G-A

142595463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38975153-A-G

142595501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38975192-A-G

142595501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38975192-A-T

142595551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38975239-A-G

142597383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38976896-A-G

142597399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38976912-G-A

142597520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38977021-G-T

142597541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38977042-T-C

http://identifiers.org/hco/5/GRCh38#142597647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38977161-C-A

142597660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38977174-G-A

142597755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38977268-A-G

http://identifiers.org/hco/5/GRCh38#142598159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38977720-A-C

142598750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978284-T-G

http://identifiers.org/hco/5/GRCh38#142598771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38978303-C-A

142598771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978303-C-T

142598788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978319-G-T

142598789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978320-T-C

142598801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978331-C-T

142598853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978396-G-C

142599041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978583-C-T

142599221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978705-A-T

142599303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978775-A-G

142599326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978789-T-C

http://identifiers.org/hco/5/GRCh38#142599344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38978809-A-C

142599554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38978982-C-G

142599784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38979190-G-A

142600062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38979473-C-G

142600062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38979473-C-T

142600393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38979800-G-T

142600613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980013-G-T

142600634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980034-C-T

142600708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38980106-G-A

142600708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, synonymous_variant
orthologous variants: 38980106-G-T

http://identifiers.org/hco/5/GRCh38#142600777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38980175-C-A

142600777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38980175-C-G

142600780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38980178-G-A

142600798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 38980196-C-T

http://identifiers.org/hco/5/GRCh38#142600877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38980275-C-A

142600877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980275-C-T

http://identifiers.org/hco/5/GRCh38#142600917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38980315-C-A

142600917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980315-C-G

142600917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980315-C-T

http://identifiers.org/hco/5/GRCh38#142601010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38980405-C-A

142601164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980532-G-A

142601164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980532-G-T

142601182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980550-A-G

http://identifiers.org/hco/5/GRCh38#142601183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38980551-A-C

142601183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980551-A-G

142601230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980594-G-A

142601230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980594-G-C

142601230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980594-G-T

142601288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980620-G-A

142601427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980750-C-T

142601437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980760-G-A

142601437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980760-G-T

142602814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38980915-T-G

142602841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980945-T-C

142602860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980964-G-A

142602861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980965-T-C

142602944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38981045-C-G

142603124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981225-G-A

142603150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38981245-C-G

http://identifiers.org/hco/5/GRCh38#142603158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38981253-C-A

142603158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38981253-C-G

142603355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981756-C-T

142603512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981835-A-G

142603566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981892-C-T

142605281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982378-T-G

142605296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982396-T-C

142605367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982478-C-T

142605571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982675-G-A

142605829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982917-G-C

142605982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983061-C-T

142605983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983062-G-A

142605983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983062-G-C

142606338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983360-C-T

142606924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983600-C-T

142606926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983602-T-C

142607045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983692-C-T

142607057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983704-A-G

142607231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38984373-G-A

http://identifiers.org/hco/5/GRCh38#142607290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38984419-C-A

142607835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38985267-C-T

142607958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38985385-C-G

142608193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986059-T-C

http://identifiers.org/hco/5/GRCh38#142608614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38986433-A-C

142608614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986433-A-T

142608615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986434-T-A

142608707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986505-A-T

142608868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986587-G-A

142608868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986587-G-C

142608922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986646-G-A

142609188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986912-A-G

142609307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987039-C-T

142609333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987065-T-C

142609443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987170-C-T

142609589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987328-C-T

142609608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987366-C-T

142609751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987482-T-C

142609760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987491-C-T

142610012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987738-G-C

142610136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987864-C-G

142610225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987949-G-A

142610428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38988154-G-A

http://identifiers.org/hco/5/GRCh38#142610690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38988360-A-C

142611290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38988840-C-T

142611320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38988856-T-C

142611398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38988931-A-T

142611478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38988990-C-T

142612500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38989866-G-A

142612655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38990322-G-T

http://identifiers.org/hco/5/GRCh38#142612856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38990486-C-A

142612912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38990525-A-G

http://identifiers.org/hco/5/GRCh38#142613830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38991475-C-A

http://identifiers.org/hco/5/GRCh38#142613858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38991503-C-A

142613858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991503-C-T

http://identifiers.org/hco/5/GRCh38#142613868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38991512-C-A

142613868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991512-C-T

142613993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38991633-T-C

http://identifiers.org/hco/5/GRCh38#142614002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38991642-C-A

142614002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38991642-C-T

142614008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38991648-G-C

142614062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38991702-A-G

142614142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38991782-T-C

142614311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991922-G-A

142614311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991922-G-C

142614365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991978-G-A

142614712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992322-T-C

142614717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992329-T-C

142614725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992334-G-A

142614873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992463-T-A

142614873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992463-T-G

142614954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992542-T-A

http://identifiers.org/hco/5/GRCh38#142614958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38992546-C-A

142615060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992712-C-T

142615121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992772-A-G

142615121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38992772-A-T

142615893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993428-A-G

142616031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993535-A-G

142616081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993564-G-A

142616133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993595-C-T

142616198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993658-T-G

142616242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993702-T-C

142616385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993837-A-T

142616420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993870-T-C

142616468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993913-A-G

142616545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993957-A-T

http://identifiers.org/hco/5/GRCh38#142616676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38994117-A-C

142616677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38994118-C-T

142616736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38994363-T-A

http://identifiers.org/hco/5/GRCh38#142616763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38994390-C-A

http://identifiers.org/hco/5/GRCh38#142616813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38994427-C-A

142616896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38994512-G-A

142617574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38995156-G-C

142617683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38995270-G-A

142617683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38995270-G-C

142618316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38995848-G-C

142618527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38996128-C-T

142618644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38996211-C-G

142618644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38996211-C-T

http://identifiers.org/hco/5/GRCh38#142618717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38996268-A-C

142618717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38996268-A-G

142618737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38996288-C-T

142619575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38996676-G-A

142620521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38998708-G-A

142620541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38998728-T-C

142620566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38998753-T-G

142620691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38998870-G-C

http://identifiers.org/hco/5/GRCh38#142621227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38999367-C-A

142621277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38999411-C-G

142621277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38999411-C-T

142621306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38999440-A-G

142621435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38999496-A-T

http://identifiers.org/hco/5/GRCh38#142621440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38999501-C-A

http://identifiers.org/hco/5/GRCh38#142621443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38999504-C-A

142621675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38999685-A-G

142621709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38999717-G-A

142622041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39000052-G-T

142622158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39000173-C-T

142622375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39000327-C-T

142622400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39000352-T-A

142622638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39000588-T-A

142622695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39000648-G-C

142623331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39001644-G-A

142623334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39001647-T-C

142624802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39002404-T-C

142624857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39002450-C-T

142624939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39002518-G-T

142625151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39002784-C-T

142625587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39003185-C-T

142626177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39003753-G-C

142626446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39003829-G-C

http://identifiers.org/hco/5/GRCh38#142626657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39004003-C-A

142626657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39004003-C-G

142626657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39004003-C-T

142626681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39004026-G-A

142626739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 39004070-G-T

142626806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39004084-T-C

142626912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39004129-A-T

http://identifiers.org/hco/5/GRCh38#142626929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39004145-C-A

142627037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39004318-C-T

http://identifiers.org/hco/5/GRCh38#142627079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39004357-C-A

142627472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39004710-G-C

http://identifiers.org/hco/5/GRCh38#142627657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39004885-C-A

142627759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39004987-G-A

142629738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006312-A-G

142629769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006350-T-C

142630090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006666-C-T

142630128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006718-G-A

142630171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006769-C-T

142630185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006783-C-T

142630560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006925-A-G

142630590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006956-G-A

142630612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39006969-C-T

142630919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39007506-T-C

142630920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39007507-G-A

142631051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39007614-T-C

142631172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39007741-T-C

142631580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39008156-C-T

142631685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39008246-G-A

142635037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39009540-C-T

142635049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39009553-A-G

142635110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39009595-A-G

http://identifiers.org/hco/5/GRCh38#142635296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39009763-A-C

142635360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39009827-C-T

142636000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010477-G-T

142636198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010624-G-T

142636273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010699-A-G

142636279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010705-C-T

142636390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010801-C-T

142636452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010862-C-T

142636472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010882-T-C

142636523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39010931-T-A

142636617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011001-A-T

http://identifiers.org/hco/5/GRCh38#142636662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39011046-C-A

142636662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011046-C-T

142636755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011124-G-A

142636755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011124-G-T

142637134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011488-G-A

142637934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011816-G-T

142637936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011818-G-A

142638014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011894-G-A

142638049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011929-G-A

142638077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39011939-G-A

142638466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39012271-G-A

142638618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39012426-G-T

142639107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39012716-A-G

142639107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39012716-A-T

142639254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39012790-G-A

142639660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013090-G-A

142639671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013101-G-A

142643027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013307-T-A

142643104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013358-T-A

142643104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013358-T-C

142643120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013374-A-G

http://identifiers.org/hco/5/GRCh38#142643152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39013424-C-A

142643152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013424-C-T

142643164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013436-A-G

142643510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39013819-C-G

142643772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39014054-G-C

142643921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39014198-C-G

142643962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39014237-C-T

142643996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39014266-A-G

http://identifiers.org/hco/5/GRCh38#142644191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39014460-C-A

142644191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39014460-C-T

http://identifiers.org/hco/5/GRCh38#142644231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39014496-C-A

142644231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39014496-C-T

http://identifiers.org/hco/5/GRCh38#142644233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39014498-C-A

http://identifiers.org/hco/5/GRCh38#142644277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39014542-C-A

142644327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39014592-C-T

142644563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39014936-G-T

http://identifiers.org/hco/5/GRCh38#142644625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39014991-A-C

http://identifiers.org/hco/5/GRCh38#142644655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#39015022-C-A

142644742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015102-G-A

142644784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015121-T-A

142644784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015121-T-C

142644870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39015205-C-T

142645025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39015356-G-C

142645444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015736-C-G

142645444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015736-C-T

142645634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015924-C-T

142645635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39015925-A-G

142645833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39016210-G-A

142646890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39016352-G-A

142651408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019197-C-G

142651416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019205-C-G

http://identifiers.org/hco/5/GRCh38#142651471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39019256-A-C

142651484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019269-T-G

142651506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019292-G-A

142651507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019293-G-T

142651728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019497-T-G

142651779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019543-G-A

142651782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019546-A-G

142651885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019645-T-C

142651917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019676-G-A

142651963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019722-T-C

http://identifiers.org/hco/5/GRCh38#142651967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39019726-C-A

142651967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019726-C-T

142651988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019747-C-T

142652028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019777-T-C

142652047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019795-C-T

http://identifiers.org/hco/5/GRCh38#142652066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39019814-A-C

142652152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39019898-G-A

142652230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020135-C-T

142652422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020320-G-T

142652462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020358-C-T

142652482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020378-C-T

142652563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020425-G-A

142652745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020544-G-A

142652759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020561-T-G

142652930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020760-T-C

142653006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39020840-G-A

142653175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021016-A-G

142653193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021033-G-T

142653210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021050-G-A

142653210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021050-G-C

142653260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021102-C-T

142653278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021110-C-T

142653397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021163-A-G

142653430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021196-C-T

142653500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021242-C-T

142653667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021443-T-A

http://identifiers.org/hco/5/GRCh38#142653674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39021450-C-A

142654127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021849-A-G

142654127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021849-A-T

142654148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39021871-T-A

http://identifiers.org/hco/5/GRCh38#142654438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39022169-C-A

http://identifiers.org/hco/5/GRCh38#142654445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39022176-C-A

142654529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39022248-T-A

142654996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39022700-C-T

142655076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39022777-C-T

142655263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39022945-G-A

http://identifiers.org/hco/5/GRCh38#142655676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39023284-C-A

142656169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39023761-A-G

http://identifiers.org/hco/5/GRCh38#142656631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39024212-C-A

142656631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39024212-C-T

142656668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39024250-G-T

142658509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39025810-G-A

142658515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39025816-A-G

142658880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39026225-C-T

142658884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39026229-G-C

142659027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39026391-T-C

142659027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39026391-T-G

142659054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39026418-G-A

142659130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39026491-T-C

142660687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028057-A-G

http://identifiers.org/hco/5/GRCh38#142660715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39028086-C-A

142660805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028196-G-A

142660973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028373-A-G

142661207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028526-C-T

142661259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028583-T-A

142661457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028785-A-G

http://identifiers.org/hco/5/GRCh38#142661464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39028792-C-A

142661521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39028850-A-G

142662144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39029086-C-T

142662168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39029110-G-A

142662375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39029304-A-G

142662427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39029349-C-G

142662486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39029408-G-A

142662502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39029429-G-A

http://identifiers.org/hco/5/GRCh38#142662520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39029447-A-C

142663641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39030321-G-A

142663737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39030403-C-T

http://identifiers.org/hco/5/GRCh38#142663754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39030419-A-C

142664049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39030714-G-T

142664061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39030726-G-A

142664198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39030872-T-C

142664250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39030908-C-T

http://identifiers.org/hco/5/GRCh38#142664425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39031051-C-A

142664425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031051-C-T

142664481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031106-A-G

142664554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031175-G-A

142664705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031305-G-A

142665907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031711-G-A

http://identifiers.org/hco/5/GRCh38#142666025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39031829-C-A

142666434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032149-C-T

142666521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032234-G-A

142666538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032251-C-G

142666578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032287-G-A

142667950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033762-G-A

142668425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39034684-C-T

142668461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39034720-C-T

142668491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39034735-G-C

http://identifiers.org/hco/5/GRCh38#142668526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39034770-A-C

142668593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39034837-G-C

142668816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39035043-G-A

http://identifiers.org/hco/5/GRCh38#142670861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39035921-C-A

142670861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39035921-C-T

142671114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39036148-C-G

142671245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39036280-T-C

142671461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39036487-A-G

142671461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39036487-A-T

142671571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39036596-T-A

142671842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39036786-G-A

http://identifiers.org/hco/5/GRCh38#142671888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39036831-C-A

http://identifiers.org/hco/5/GRCh38#142671972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39036896-C-A

142671972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39036896-C-T

142673309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39038426-G-T

142673722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39038795-T-C

142673746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39038806-G-A

142673746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39038806-G-T

142673832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39038844-C-T

142673854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39038864-A-T

142674321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39039305-C-T

142674322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39039306-G-A

142674667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39039641-A-G

http://identifiers.org/hco/5/GRCh38#142675020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39040577-C-A

142675288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39040855-G-A

142675423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39040995-G-A

142675693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041238-C-T

142675758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041292-C-T

142675864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041394-G-A

142675873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041403-T-C

142675921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041446-T-A

142675921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041446-T-C

http://identifiers.org/hco/5/GRCh38#142675949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39041470-A-C

142676000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041520-G-A

142676000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041520-G-T

142676265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39041890-A-G

142676598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39042217-C-T

142676611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39042229-G-C

http://identifiers.org/hco/5/GRCh38#142676844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39042297-C-A

142676883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39042334-A-T

142677164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39042493-C-T

142677583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39042910-C-G

142677583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39042910-C-T

142677624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043015-C-T

142677629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043043-C-T

142677945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043344-C-G

142678140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043512-G-A

142678182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043525-T-C

142678249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043569-A-G

142678330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043651-G-A

142678398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043732-T-C

142678418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39043751-G-A

142678527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39044007-C-T

142679207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39045434-A-G

142679402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39045567-G-A

142679501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39045640-G-T

142679777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39045923-G-A

142679777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39045923-G-T

http://identifiers.org/hco/5/GRCh38#142680105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39046168-C-A

142680105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046168-C-T

142680129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046192-T-C

142680158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046220-T-C

142680187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046249-A-G

http://identifiers.org/hco/5/GRCh38#142680375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39046340-C-A

142680402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046367-G-A

142680538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046485-T-C

142680627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046580-A-G

142680678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39046594-C-G

142680722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39046636-G-T

http://identifiers.org/hco/5/GRCh38#142680754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#39046657-C-A

http://identifiers.org/hco/5/GRCh38#142680858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#39046758-C-A

142680858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39046758-C-G

142681518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39047849-G-A

http://identifiers.org/hco/5/GRCh38#142681626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39047957-C-A

142681713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39048015-G-A

http://identifiers.org/hco/5/GRCh38#142681784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39048076-C-A

142681793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39048084-T-G

142682826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39048997-T-C

142683066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049204-T-C

142684178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049437-C-T

http://identifiers.org/hco/5/GRCh38#142684260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39049518-C-A

142684260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049518-C-T

142684325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049583-G-A

http://identifiers.org/hco/5/GRCh38#142684358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39049602-C-A

http://identifiers.org/hco/5/GRCh38#142684376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39049619-C-A

142684419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049633-T-C

142684419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049633-T-G

http://identifiers.org/hco/5/GRCh38#142684481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39049689-A-C

142684481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39049689-A-T

142685007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39050813-T-C

142685054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39050855-G-A

142685248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39050994-G-A

142685274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051018-G-T

142685463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051167-A-G

142685463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051167-A-T

http://identifiers.org/hco/5/GRCh38#142685533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39051226-C-A

142685533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051226-C-G

142685533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051226-C-T

142685543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051236-G-A

142685700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051379-G-T

142685735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051413-T-C

142685763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051440-G-A

142685763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051440-G-T

142685793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051469-T-C

http://identifiers.org/hco/5/GRCh38#142685811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39051486-C-A

http://identifiers.org/hco/5/GRCh38#142686058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39051720-C-A

142686058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051720-C-G

142686058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051720-C-T

142686060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051722-G-A

142686060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39051722-G-T

142686124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051786-T-C

http://identifiers.org/hco/5/GRCh38#142686226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39051864-C-A

142686226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051864-C-T

http://identifiers.org/hco/5/GRCh38#142686344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39051992-C-A

142686344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39051992-C-G

142686457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39052077-G-A

142686478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39052098-T-A

142686478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39052098-T-C

142686770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39052366-G-A

142686775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39052371-G-A

142687094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39052649-G-A

142687138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39052723-C-T

142687144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39052729-C-T

http://identifiers.org/hco/5/GRCh38#142687908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39054914-C-A

142687908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39054914-C-G

142687925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39054930-T-C

142687959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39054963-C-T

142688182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39055162-T-G

142688183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39055163-G-A

142688256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39055239-G-A

http://identifiers.org/hco/5/GRCh38#142688618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39055636-C-A

142689082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39056085-G-A

142689820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39056716-T-A

142689829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39056724-G-T

http://identifiers.org/hco/5/GRCh38#142689830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39056725-C-A

http://identifiers.org/hco/5/GRCh38#142689836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39056731-C-A

142689896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39056816-T-A

142689950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39056875-C-T

142692677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058066-G-A

142692677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058066-G-C

142692705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058094-A-G

142692922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058248-G-C

142693030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058362-T-C

http://identifiers.org/hco/5/GRCh38#142693131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39058431-C-A

142693261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058569-C-T

142693282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058612-T-A

http://identifiers.org/hco/5/GRCh38#142693623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39058978-C-A

142693624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39058979-T-G

http://identifiers.org/hco/5/GRCh38#142693714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#39059048-C-A

142693889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059217-G-A

142693909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059234-C-T

142694847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059469-G-A

142694944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059573-T-C

142694988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059619-C-T

142695026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059657-T-C

142695067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059695-T-A

142695111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059737-G-A

142695746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059971-T-G

142695747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39059972-G-C

142696154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39060479-C-T

142696285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39060575-T-C

142696691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39061327-T-A

142696693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39061329-C-T

142696923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39061537-G-A

142697480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39062057-A-G

142697541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39062113-A-G

142697682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062211-A-G

142697682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062211-A-T

142697785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062315-T-C

142697813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062336-T-C

142697862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062379-G-A

142697862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062379-G-T

142697932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062444-C-T

142697941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062453-G-A

142697986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3665
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39062501-G-T