http://identifiers.org/hco/4/GRCh38#959015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108795056-C-A

959201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795237-G-A

959201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795237-G-T

959205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795241-A-G

http://identifiers.org/hco/4/GRCh38#959208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108795244-A-C

959208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795244-A-G

http://identifiers.org/hco/4/GRCh38#959227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108795260-C-A

959227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795260-C-T

959239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795270-G-A

959239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795270-G-T

959327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795389-G-T

959334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795430-G-A

959334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795430-G-T

959435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795589-G-C

959435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795589-G-T

959568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795687-G-A

959568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795687-G-T

959590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795707-A-G

959602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795712-G-A

959602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795712-G-T

959608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795718-G-A

959608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795718-G-T

http://identifiers.org/hco/4/GRCh38#959616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108795726-C-A

959616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795726-C-G

959616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795726-C-T

959624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795730-G-A

959624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795730-G-T

http://identifiers.org/hco/4/GRCh38#959630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108795735-C-A

http://identifiers.org/hco/4/GRCh38#959685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108795791-C-A

959685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795791-C-T

959756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795854-G-A

959756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795854-G-C

959756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795854-G-T

959762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108795860-C-T

http://identifiers.org/hco/4/GRCh38#959926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108796021-A-C

959926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796021-A-G

959944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796038-G-A

959944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796038-G-C

959944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796038-G-T

http://identifiers.org/hco/4/GRCh38#959974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108796064-C-A

959974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796064-C-T

960014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796101-A-G

960455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796448-G-A

960455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796448-G-C

960455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796448-G-T

960531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796523-G-A

960531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3 prime UTR variant
orthologous variants: 108796523-G-T

960628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense variant
orthologous variants: 108796584-G-T

960672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense variant
orthologous variants: 108796628-G-T

960808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796750-G-A

960808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796750-G-T

960813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796755-T-C

960862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796811-G-A

960881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796824-G-A

960902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796852-G-C

960902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796852-G-T

961031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108796994-C-T

http://identifiers.org/hco/4/GRCh38#961444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108797223-C-A

961444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797223-C-T

961456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797233-C-G

961456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797233-C-T

961563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108797340-G-A

961563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108797340-G-T

961656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797426-C-T

http://identifiers.org/hco/4/GRCh38#961756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108797521-C-A

961845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797611-G-A

http://identifiers.org/hco/4/GRCh38#961853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108797619-C-A

961876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797645-A-G

http://identifiers.org/hco/4/GRCh38#962116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108797821-C-A

962116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108797821-C-T

http://identifiers.org/hco/4/GRCh38#962412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108798055-C-A

962412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108798055-C-G

962412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108798055-C-T

http://identifiers.org/hco/4/GRCh38#962470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108798102-C-A

962470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense variant
orthologous variants: 108798102-C-T

962540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 108798172-A-G

http://identifiers.org/hco/4/GRCh38#962704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108798290-C-A

962967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108798567-A-G

962967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108798567-A-T

963408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798942-T-C

963408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798942-T-G

963422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798947-T-A

963422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798947-T-C

963422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108798947-T-G

963923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799360-G-A

963923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799360-G-C

963923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799360-G-T

963953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799386-A-G

963953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799386-A-T

963960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799393-G-A

963960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799393-G-T

http://identifiers.org/hco/4/GRCh38#963970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108799403-A-C

963970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799403-A-G

963998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799425-G-A

963998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799425-G-T

http://identifiers.org/hco/4/GRCh38#964009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108799436-C-A

964009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799436-C-T

http://identifiers.org/hco/4/GRCh38#964056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108799482-C-A

964056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 108799482-C-T

http://identifiers.org/hco/4/GRCh38#964082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108799505-C-A

964082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108799505-C-T

964124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108799527-C-T

964883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800061-G-T

965023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800179-C-T

http://identifiers.org/hco/4/GRCh38#965044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108800200-C-A

965044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800200-C-T

965097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800226-G-A

965097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800226-G-T

965150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800241-A-G

965350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108800439-G-A

965836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801412-G-A

965836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801412-G-C

965836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801412-G-T

965854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801434-G-A

965854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108801434-G-T

966024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 108801598-C-T

http://identifiers.org/hco/4/GRCh38#966154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108801731-C-A

966178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801742-G-A

966178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801742-G-C

http://identifiers.org/hco/4/GRCh38#966210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108801776-C-A

966210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801776-C-T

http://identifiers.org/hco/4/GRCh38#966223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108801789-C-A

966295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801855-G-A

966295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801855-G-C

966295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108801855-G-T

966296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108801856-G-A

966296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108801856-G-C

966296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108801856-G-T

966517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802001-C-G

966517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802001-C-T

http://identifiers.org/hco/4/GRCh38#966586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108802068-C-A

966586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802068-C-T

http://identifiers.org/hco/4/GRCh38#966617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108802099-C-A

966617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802099-C-T

966628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802119-T-C

966661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802152-G-A

966661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802152-G-C

966661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802152-G-T

966791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802265-G-A

966791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802265-G-C

966791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802265-G-T

966814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802282-G-A

966814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802282-G-C

966866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802338-G-A

966866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802338-G-T

966888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802348-T-C

966907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802367-G-A

966907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108802367-G-T

http://identifiers.org/hco/4/GRCh38#967015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108802461-C-A

967015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802461-C-T

967175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108802628-G-A

967175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108802628-G-C

967175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108802628-G-T

967202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense variant
orthologous variants: 108802655-T-A

967202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: missense variant
orthologous variants: 108802655-T-C

967344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108802785-G-A

967344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108802785-G-C

967344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108802785-G-T

967353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108802794-T-C

967353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108802794-T-G

967376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802811-G-A

967376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802811-G-T

967385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802820-G-A

967385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802820-G-T

967391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802822-T-A

967391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802822-T-C

967391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802822-T-G

967431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802866-G-A

967431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802866-G-T

967451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802885-T-C

967451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802885-T-G

967454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802888-G-A

967454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802888-G-C

967454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802888-G-T

967498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802935-G-A

967498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802935-G-C

967498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108802935-G-T

967618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108803043-G-A

967655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 108803080-C-G

967780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: synonymous variant
orthologous variants: 108803208-G-A

968047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108803493-A-G

http://identifiers.org/hco/4/GRCh38#968086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108803548-C-A

968086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108803548-C-T

http://identifiers.org/hco/4/GRCh38#968267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108803692-C-A

968267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108803692-C-G

968267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108803692-C-T

968633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108804067-T-C

968633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108804067-T-G

968913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108804392-G-A

968996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804536-G-A

968996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108804536-G-T

969368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108804792-G-T

969515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108804907-C-G

969545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108804934-T-C

969555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108804944-T-G

http://identifiers.org/hco/4/GRCh38#970861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108805957-C-A

970861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108805957-C-T

970896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108805994-A-G

970896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108805994-A-T

http://identifiers.org/hco/4/GRCh38#970925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108806030-C-A

970925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108806030-C-T

http://identifiers.org/hco/4/GRCh38#970926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108806031-C-A

970926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108806031-C-T

http://identifiers.org/hco/4/GRCh38#971318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108806386-A-C

971318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108806386-A-G

971804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108806681-C-T

972145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108806988-G-A

972145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108806988-G-T

972188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108807056-G-A

972962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108808026-G-A

http://identifiers.org/hco/4/GRCh38#973195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108808267-C-A

973195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108808267-C-G

973195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108808267-C-T

973320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant
orthologous variants: 108808414-G-A

973320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, missense_variant
orthologous variants: 108808414-G-T

http://identifiers.org/hco/4/GRCh38#973322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: coding_sequence_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108808416-C-A

973322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: coding_sequence_variant, intron_variant, missense_variant
orthologous variants: 108808416-C-G

973322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: coding_sequence_variant, intron_variant, missense_variant
orthologous variants: 108808416-C-T

973390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108808469-T-A

973390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108808469-T-C

973429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 108808508-C-T

http://identifiers.org/hco/4/GRCh38#973491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108808570-C-A

http://identifiers.org/hco/4/GRCh38#973551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#108808638-C-A

973551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 108808638-C-G

973551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 108808638-C-T

http://identifiers.org/hco/4/GRCh38#973660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#108808732-A-C

973660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2856
most severe consequence: intron variant
orthologous variants: 108808732-A-G