http://identifiers.org/hco/7/GRCh38#55019020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702233-C-A

55019020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 16702233-C-G

55019020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 16702233-C-T

55019039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 16702251-G-A

55019039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 16702251-G-C

55019039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 16702251-G-T

55019069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5 prime UTR variant
orthologous variants: 16702284-G-A

55019069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5 prime UTR variant
orthologous variants: 16702284-G-C

55019069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5 prime UTR variant
orthologous variants: 16702284-G-T

http://identifiers.org/hco/7/GRCh38#55019132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702337-C-A

55019132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702337-C-T

http://identifiers.org/hco/7/GRCh38#55019152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702356-A-C

55019152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702356-A-G

55019152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702356-A-T

http://identifiers.org/hco/7/GRCh38#55019181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702382-C-A

55019181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702382-C-T

55019245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702451-G-A

55019245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702451-G-C

55019245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16702451-G-T

http://identifiers.org/hco/7/GRCh38#55019317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702522-C-A

55019317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16702522-C-T

http://identifiers.org/hco/7/GRCh38#55019390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702593-C-A

55019390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702593-C-G

55019390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702593-C-T

http://identifiers.org/hco/7/GRCh38#55019422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702609-C-A

55019422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702609-C-T

http://identifiers.org/hco/7/GRCh38#55019434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702621-C-A

55019434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702621-C-T

http://identifiers.org/hco/7/GRCh38#55019455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16702644-C-A

55019455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702644-C-G

55019455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702644-C-T

55019521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702697-G-C

55019635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16702814-G-C

55019878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703035-C-T

55019938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703107-G-A

55019940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703109-A-G

55020052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703216-C-G

55020057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703224-C-G

55020129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16703317-T-A

55020129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16703317-T-C

55020193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16703363-T-G

55020253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703420-G-A

55020258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703425-A-G

55020461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16703577-C-T

55020499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703616-C-G

55020781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16703900-G-A

55020954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16704076-A-G

55021435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16704472-A-G

http://identifiers.org/hco/7/GRCh38#55021790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16704831-A-C

55021876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16704921-G-A

55021881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16704926-G-A

http://identifiers.org/hco/7/GRCh38#55022051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16705066-C-A

55022051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705066-C-T

55022083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705093-G-C

http://identifiers.org/hco/7/GRCh38#55022369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16705331-C-A

55022410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705378-C-T

http://identifiers.org/hco/7/GRCh38#55022414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16705382-C-A

55022462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705442-C-T

55022500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705481-G-A

55022500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705481-G-C

55022669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705678-G-A

55022687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705702-G-A

55022699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705715-C-T

55024339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705962-G-C

55024372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705994-G-A

55024372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16705994-G-T

55024576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706162-C-T

55024686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706258-T-C

55024724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706296-A-G

55024820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706394-A-G

55024991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706522-G-T

55025019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706554-C-T

55025223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706750-G-A

55025318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16706839-G-A

55025690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16707159-C-T

55025714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16707173-T-G

55025715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16707174-G-C

http://identifiers.org/hco/7/GRCh38#55025794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16707258-A-C

55025794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16707258-A-G

http://identifiers.org/hco/7/GRCh38#55027161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16707545-C-A

55027489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16707875-C-T

55027806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16708189-T-A

55027806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16708189-T-C

55027942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16708296-G-A

http://identifiers.org/hco/7/GRCh38#55028512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16708935-C-A

55028598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16709028-A-G

55028692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16709125-T-C

55030517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16709458-C-T

55030718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16709662-A-G

http://identifiers.org/hco/7/GRCh38#55030806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16709831-A-C

http://identifiers.org/hco/7/GRCh38#55031082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16710240-A-C

55031226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16710388-G-A

55031405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16710561-T-C

55031490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16710631-T-C

55032502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16711343-G-A

55032850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16711700-G-A

55032850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16711700-G-C

55032850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16711700-G-T

55033032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16711852-A-G

http://identifiers.org/hco/7/GRCh38#55034878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16713960-A-C

55034878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16713960-A-G

55034889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16713971-C-T

55035031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714100-A-G

55035040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714108-G-C

55035040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714108-G-T

http://identifiers.org/hco/7/GRCh38#55035062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16714130-C-A

55035062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714130-C-T

55035089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714156-A-T

55035143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714195-G-A

55035462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714497-T-C

55035463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714498-G-A

55035463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714498-G-T

55035623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714646-T-G

55035754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714758-A-T

55035859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714900-A-G

55035862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16714914-C-T

55036222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715234-C-T

55036296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715302-G-T

55036297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715303-T-G

55036498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715505-T-C

55036584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715674-G-A

55036826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715984-G-A

55036827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16715985-G-A

55036951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716117-T-C

55036998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716164-G-C

55037143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716312-G-A

55037220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716375-A-G

55037289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716435-T-A

55037316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716457-A-G

55037397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716538-A-G

55037400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716541-A-G

http://identifiers.org/hco/7/GRCh38#55037814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16716959-C-A

55037814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16716959-C-T

55039828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16717909-G-A

55040042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718078-G-A

55040042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718078-G-C

55040042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718078-G-T

55040386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718358-G-A

55040386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718358-G-T

http://identifiers.org/hco/7/GRCh38#55040546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16718509-A-C

55040604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718553-G-T

55040767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16718685-C-T

55043742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16719265-A-G

http://identifiers.org/hco/7/GRCh38#55043765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16719293-C-A

55043766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16719294-A-G

http://identifiers.org/hco/7/GRCh38#55043777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16719314-C-A

55043777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16719314-C-T

http://identifiers.org/hco/7/GRCh38#55043818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16719355-C-A

55044041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16719572-T-A

55044211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16719756-A-G

http://identifiers.org/hco/7/GRCh38#55044561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16720071-C-A

55044561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16720071-C-G

55044561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16720071-C-T

55044699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16720209-T-C

55044786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16720297-C-T

55044842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16720353-C-G

55044987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16720476-A-G

http://identifiers.org/hco/7/GRCh38#55045299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16721545-A-C

55045344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16721586-T-A

55045362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16721604-A-G

55045389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16721629-C-T

55045569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16721806-C-T

55046163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16722549-T-C

55046202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16722585-G-A

55046478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16722809-C-T

55046519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16722850-G-A

55046557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16722887-G-A

55046927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16724897-T-A

55048088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16725811-T-C

55048176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16725908-C-T

55048236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16725980-C-T

55048626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16726288-G-A

55049079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16726690-G-A

55049140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16726752-T-C

55049140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16726752-T-G

55049703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16727263-G-A

55049709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16727269-G-T

http://identifiers.org/hco/7/GRCh38#55049759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16727313-A-C

55049759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16727313-A-G

55050191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728144-A-G

http://identifiers.org/hco/7/GRCh38#55050551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16728423-A-C

55050599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728470-C-T

http://identifiers.org/hco/7/GRCh38#55050648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16728519-A-C

http://identifiers.org/hco/7/GRCh38#55050653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16728524-C-A

55050666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728537-C-G

55050670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728541-C-T

55052904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728953-T-G

55052920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728969-G-A

55052932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16728980-G-A

55053046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729071-T-G

55053292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729340-C-T

55053398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729446-G-A

55053463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16729507-G-A

http://identifiers.org/hco/7/GRCh38#55054399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16731400-A-C

55054535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731524-G-C

55054591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731567-A-T

55054647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731620-T-A

55054685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731655-G-A

55054706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731674-T-C

55054706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731674-T-G

55054721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731693-G-A

55054724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731696-G-C

55054993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731861-C-T

55055057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16731909-A-G

55055296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732106-C-T

55055342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732152-G-A

55055350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732160-G-A

http://identifiers.org/hco/7/GRCh38#55055365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16732176-C-A

55055365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732176-C-T

55055461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732248-C-T

55055469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732255-T-C

55055626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732386-G-A

55055626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732386-G-T

55055641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732397-G-A

http://identifiers.org/hco/7/GRCh38#55055769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16732478-C-A

55055769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732478-C-G

55055888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732598-A-G

55055907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732617-A-T

55056081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16732783-C-T

55056320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16733627-C-T

55056330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16733637-T-C

55056607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16733911-A-G

55056723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16734027-G-A

55056725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16734029-C-G

55056725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16734029-C-T

55056993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16734307-A-G

55056993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16734307-A-T

http://identifiers.org/hco/7/GRCh38#55057089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16734387-A-C

http://identifiers.org/hco/7/GRCh38#55057116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16734414-C-A

55057571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16734833-T-G

55060644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736437-C-T

55060645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736438-A-G

55060645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736438-A-T

55060735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736517-A-G

http://identifiers.org/hco/7/GRCh38#55060742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16736524-C-A

55060742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736524-C-T

55061060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736712-T-C

55061355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736991-T-C

55061356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16736992-G-C

55061496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16737119-T-C

55062756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16738314-G-A

55062889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16738445-G-A

55063371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16738924-C-G

http://identifiers.org/hco/7/GRCh38#55063678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16739201-A-C

55063707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16739230-G-A

55064262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16739590-A-G

55064262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16739590-A-T

55064308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16739621-G-A

55064526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16739823-A-T

55065210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16740359-T-G

55065213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16740362-C-T

55065398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16740546-T-C

55065437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16740583-C-T

55065459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16740605-G-T

55065671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741195-T-C

http://identifiers.org/hco/7/GRCh38#55065730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16741258-A-C

55065815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741330-T-C

http://identifiers.org/hco/7/GRCh38#55065822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16741337-C-A

55065822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741337-C-T

55065870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741367-T-C

55066195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741701-G-A

55066253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741761-C-G

55066472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16741959-C-T

55066679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742175-T-C

55066728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742219-A-G

55066810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742326-G-A

55066929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742423-A-T

http://identifiers.org/hco/7/GRCh38#55068838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16742667-C-A

55068838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742667-C-T

55068921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742730-G-A

55069173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742977-T-A

55069173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742977-T-C

55069174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16742978-G-A

http://identifiers.org/hco/7/GRCh38#55070074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16743393-C-A

55070386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16743676-A-G

55070733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16743993-T-C

55070971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16744131-C-T

55071018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16744167-C-T

http://identifiers.org/hco/7/GRCh38#55071028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16744176-C-A

55071157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16744314-G-A

55071321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16744482-G-A

http://identifiers.org/hco/7/GRCh38#55071341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16744502-C-A

55071750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16744985-A-T

55071953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16745175-T-C

55071978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16745200-G-T

55072089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16745410-G-A

55072483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16745796-G-A

55072483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16745796-G-C

55073021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746037-A-G

55073100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746113-A-G

55073139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746152-T-G

55073503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16745410-A-G

55074256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746711-T-C

55074266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16746722-C-T

http://identifiers.org/hco/7/GRCh38#55074644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16747088-A-C

55074964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747331-T-C

55075031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747396-T-C

55075121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747482-C-G

55075143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16747498-G-C

55075503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748049-C-T

55075609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748161-G-A

55075636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748188-T-C

55075881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748428-T-A

55075905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16748452-A-G

55076698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749490-T-G

55076733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749519-G-A

55076838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749644-A-G

55077047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749845-G-A

55077047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749845-G-T

55077110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749909-T-A

55077110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16749909-T-G

55077402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16750164-T-C

55077888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16750653-G-A

55077997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16750777-A-T

55078355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751111-C-G

55078484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751226-G-A

55078584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751322-C-T

55078585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751323-G-C

http://identifiers.org/hco/7/GRCh38#55078615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16751346-C-A

55078623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751354-C-T

55078701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751424-G-T

55078706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751429-G-C

55078741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751464-C-T

55078833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751548-C-G

55078973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751695-G-A

55079103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751752-G-A

55079129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751772-G-C

55079134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751777-G-A

55079144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751787-G-A

http://identifiers.org/hco/7/GRCh38#55079172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#16751826-C-A

55079172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751826-C-T

55079183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751833-A-G

55079205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751867-G-A

55079218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751880-A-G

http://identifiers.org/hco/7/GRCh38#55079231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#16751895-C-A

55079231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751895-C-T

55079255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16751910-G-A

55079311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16751963-G-A

55079377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16752026-T-C

55079592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16752263-G-T

55080263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16753219-T-G

55080306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16753223-G-T

55080440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16753332-G-A

55080443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16753335-C-T

55080676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16753553-A-G

55080727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16753610-T-C

55080733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16753616-C-T

http://identifiers.org/hco/7/GRCh38#55080734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16753617-A-C

55080793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16753675-A-T

55080798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16753680-A-G

55080908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16753786-T-G

http://identifiers.org/hco/7/GRCh38#55081366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16754237-C-A

55081665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16754529-G-A

55081668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16754532-A-T

55082102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16755926-T-C

55082159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16755983-A-G

55082206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756032-G-A

55082225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16756049-G-C

55082551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756321-T-C

55082576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756365-G-A

55082668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756430-G-A

55082758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756539-C-T

55082846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756629-C-T

55082888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756665-C-T

55083218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16756979-G-A

55083351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16757087-A-G

55083359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16757095-G-T

55083517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16757245-T-C

55086128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16759065-C-T

55086172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16759105-A-G

55086238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16759145-G-T

http://identifiers.org/hco/7/GRCh38#55086358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16759305-C-A

55086503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16759434-T-C

55086876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16759616-G-A

55087044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16759742-G-A

http://identifiers.org/hco/7/GRCh38#55087396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16759974-C-A

55087411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16759987-G-C

55087517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760097-G-A

55087517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760097-G-T

55087541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760121-G-A

55088271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760512-T-C

55088282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760523-C-T

55088375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760618-G-A

55088378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760621-G-A

55088401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760639-A-G

55088406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760644-A-T

55088484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760732-A-T

55088532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16760780-G-A

http://identifiers.org/hco/7/GRCh38#55088624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16760872-C-A

55088789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761057-G-A

55088815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761172-T-C

55088834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761200-A-G

55088915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761281-C-G

55089232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761610-C-G

55089311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761699-G-A

55089387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761782-T-C

55089538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16761927-A-G

55089711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16762086-T-C

http://identifiers.org/hco/7/GRCh38#55089812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16762181-C-A

55090259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16762326-C-G

55090332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16762400-G-A

http://identifiers.org/hco/7/GRCh38#55090567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16762620-A-C

55090703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16762910-T-C

55090741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16762996-C-T

55090898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16763232-C-T

55090914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16763242-T-C

55091091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16763413-T-A

55091536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16763701-C-T

55092201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16764338-G-C

55092400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16764493-T-C

http://identifiers.org/hco/7/GRCh38#55092635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16764712-C-A

55092845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16764907-A-G

55092915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16764977-T-A

55092985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765051-A-G

55093030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765094-C-T

http://identifiers.org/hco/7/GRCh38#55093075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16765219-C-A

55093163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765311-C-T

55093164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765312-C-T

55093254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765382-G-C

55093339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765490-G-C

55093382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765532-G-A

55093382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765532-G-T

55093556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765695-C-G

55093556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16765695-C-T

http://identifiers.org/hco/7/GRCh38#55093572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16765711-C-A

55093683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766010-G-A

55093727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766075-T-A

55094015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766365-A-G

55094124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766475-G-A

55094452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766777-G-A

55094462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766787-G-A

55094612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16766919-A-G

http://identifiers.org/hco/7/GRCh38#55095991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16768468-A-C

55096105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16768571-C-T

http://identifiers.org/hco/7/GRCh38#55096130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16768597-A-C

55096209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16768668-T-C

http://identifiers.org/hco/7/GRCh38#55096812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16769108-C-A

55096812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769108-C-T

55096885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769192-A-G

55096965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769278-A-G

http://identifiers.org/hco/7/GRCh38#55096984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16769297-A-C

55097014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769328-T-A

55097020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769334-G-A

55098688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769780-C-T

55098800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769885-C-T

55098822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769906-A-G

55098834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769918-T-C

55098861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769940-G-A

55098908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16769990-C-G

55098990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770084-G-A

http://identifiers.org/hco/7/GRCh38#55099021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16770113-C-A

55099046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770137-C-T

http://identifiers.org/hco/7/GRCh38#55099102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16770190-C-A

55099260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770336-C-G

55099437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770502-C-T

55099521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770579-G-A

55099521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770579-G-T

55099690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770760-A-G

55099764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16770841-A-G

55099825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770902-T-A

55099923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16770987-C-G

55099929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16770993-C-T

55100114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16771563-T-C

55100306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16771753-A-G

55101361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16772857-C-T

55101484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16772973-C-T

55101515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16773004-C-T

http://identifiers.org/hco/7/GRCh38#55101572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16773183-C-A

55101573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16773184-C-T

55101743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16773375-T-C

http://identifiers.org/hco/7/GRCh38#55101894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16773519-C-A

http://identifiers.org/hco/7/GRCh38#55102167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16773746-C-A

http://identifiers.org/hco/7/GRCh38#55102509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16774031-C-A

55103902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16774096-G-A

55103984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16774193-G-C

55103984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16774193-G-T

55104212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16774430-T-C

55104251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16774471-G-A

http://identifiers.org/hco/7/GRCh38#55104406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16774588-A-C

55104535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16774714-G-T

55104781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16775074-T-C

http://identifiers.org/hco/7/GRCh38#55104910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16775211-C-A

55105406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16775717-C-T

55105547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16775851-C-T

55106045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16776452-G-A

http://identifiers.org/hco/7/GRCh38#55106085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16776496-A-C

55106503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16777038-C-G

55106503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16777038-C-T

55106591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16777120-C-G

55106826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16777778-T-A

55106886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16777833-C-T

55107105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16777949-T-C

55107278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16778098-C-T

55107426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16778210-G-A

55107566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16778338-C-T

http://identifiers.org/hco/7/GRCh38#55107575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16778347-C-A

55107646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16778415-G-T

55108372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16779587-G-A

http://identifiers.org/hco/7/GRCh38#55108939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16780049-A-C

55109585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16780729-A-G

55109679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16780822-T-C

55109703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16780846-T-C

55109703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16780846-T-G

55109747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16780890-C-T

55109791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16780939-T-C

55109829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16780969-G-A

55109899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781042-G-A

55109899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781042-G-C

55109899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781042-G-T

55109908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781051-T-A

55109908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781051-T-C

55109908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781051-T-G

http://identifiers.org/hco/7/GRCh38#55109924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16781067-C-A

55109924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781067-C-T

55109977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781118-A-T

55109998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781136-A-G

55110375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781618-A-G

55110429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781677-A-G

http://identifiers.org/hco/7/GRCh38#55110552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16781801-C-A

55110552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781801-C-T

55110643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16781892-A-G

55110881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16782126-T-C

55111011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16782255-T-C

55111152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16782400-G-A

55111162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16782410-C-T

55111515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16782721-G-T

55111569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16782765-C-G

55111962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16783157-G-C

55112278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16783496-G-C

55112278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16783496-G-T

55112392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16783646-G-A

55112424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16783679-A-G

55112543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16783802-G-A

55112942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16784271-T-C

55113081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16784388-A-T

http://identifiers.org/hco/7/GRCh38#55113548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16784768-C-A

55113574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16784789-G-A

55113595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16784809-C-G

55113595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16784809-C-T

55113979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16785175-G-A

http://identifiers.org/hco/7/GRCh38#55114094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16785294-C-A

55114569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16785550-C-T

55115227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16785875-C-G

55115434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786054-T-G

55115759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786384-G-A

55115868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786496-C-G

55116143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786734-G-C

55116143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786734-G-T

55116250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786810-C-T

55116330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16786882-C-T

55116637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16787092-A-G

55116744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16787180-T-C

55116846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16787283-C-T

55116851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16787288-C-G

55116935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16787379-G-A

55117472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16788665-G-C

55117791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16788937-C-G

55118014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16789133-G-A

55118103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16789244-A-G

55120254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16789497-C-T

http://identifiers.org/hco/7/GRCh38#55120363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16789598-A-C

55120452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16789697-G-A

55121009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791004-G-A

55121009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791004-G-C

55121167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791142-T-C

55121389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791373-C-T

http://identifiers.org/hco/7/GRCh38#55121444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16791426-A-C

55121458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791440-C-T

55121609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791592-C-T

55121863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16791814-C-T

55122207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792216-G-C

55122271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792276-G-T

http://identifiers.org/hco/7/GRCh38#55122292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16792292-C-A

55122339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792334-C-T

55122444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792459-G-A

55122483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792520-G-A

55122513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792570-T-A

55122513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792570-T-C

55122905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792899-G-A

55122946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792930-T-C

55123003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16792985-A-T

55123029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793011-G-A

55123123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793108-G-A

55126909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793295-A-G

55127005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793389-G-C

55127043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793426-A-T

55127170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793525-A-G

55127230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793585-T-A

55127237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793592-C-T

55127314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793671-G-A

55127325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793682-T-C

55127346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793702-T-C

http://identifiers.org/hco/7/GRCh38#55127408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16793754-C-A

55127496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16793843-A-T

55127917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16794255-A-G

55128079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16794425-A-G

55128150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16794481-C-G

http://identifiers.org/hco/7/GRCh38#55128318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16794680-A-C

55128412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16794718-G-C

55129131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795281-C-T

55129164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795309-C-T

55129182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795326-G-A

55129182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795326-G-T

55129285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795404-G-A

55129314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795433-G-A

55129385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795503-G-C

55129385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795503-G-T

55129446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795563-A-G

55129522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795610-G-A

55129560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795644-G-A

55129743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16795783-T-C

55130347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16798362-T-C

55130518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16798559-C-G

55130544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16798586-G-A

55130762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16798840-G-C

55130807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16798915-G-A

55130807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16798915-G-C

55130953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799091-G-A

55131185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799348-T-C

55131303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799468-C-T

55131599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799710-G-A

55131599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799710-G-C

55131601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799712-A-G

55131949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799868-A-G

55132066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799899-C-T

55132145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16799975-T-C

55132350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800160-T-G

55132673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800449-T-C

55132702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800483-A-G

55132731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800504-G-A

55132731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800504-G-T

55132734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800507-T-G

55132857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16800991-A-G

http://identifiers.org/hco/7/GRCh38#55132955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16801087-A-C

55133483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16801636-T-C

55133552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16801704-G-T

55133612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16801760-T-A

55133616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16801764-G-T

55133635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16801783-C-T

55133945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16802227-C-T

55134117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16802383-T-A

55134879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16803040-C-T

55137628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16804298-T-A

55137761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16804416-T-C

http://identifiers.org/hco/7/GRCh38#55137835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16804484-C-A

55137835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16804484-C-T

55137881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16804531-C-G

55138088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16804680-G-A

55138211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16804787-T-C

55138706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16805309-T-G

55138735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16805337-G-A

55139556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806074-G-A

55139580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806096-A-G

55139580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806096-A-T

55139619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806133-T-C

55139671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806185-G-A

55139765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806301-G-A

55139964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806490-T-C

55140323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806742-G-T

55140577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16806983-T-C

55140713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16807102-T-C

55140739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807128-G-C

55140909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807278-A-G

55140954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807330-G-A

55140954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807330-G-T

55141025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807394-T-C

http://identifiers.org/hco/7/GRCh38#55141041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16807411-A-C

55141130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807503-G-T

55141405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807777-G-A

55141461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807809-G-A

http://identifiers.org/hco/7/GRCh38#55141489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16807837-C-A

55141535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16807884-G-A

55141766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16808120-G-A

55141796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16808148-G-A

http://identifiers.org/hco/7/GRCh38#55141837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16808188-A-C

55141967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16808665-A-T

http://identifiers.org/hco/7/GRCh38#55142146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16808827-C-A

55142271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16808878-G-A

55142271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16808878-G-C

55142412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16809022-G-C

55142524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809235-T-C

55142525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809236-T-A

55142525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809236-T-G

55142537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809249-T-C

55142538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809250-G-A

http://identifiers.org/hco/7/GRCh38#55142555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16809275-C-A

55142555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809275-C-T

http://identifiers.org/hco/7/GRCh38#55142560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16809280-C-A

55142579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809382-G-A

55142739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809556-T-C

55142777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809604-A-G

55142993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809810-G-A

55143179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809968-A-T

55143194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16809978-G-A

55143230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16810009-C-G

55143263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16810032-T-C

55143290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16810051-G-A

55143365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16810128-T-C

55143476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16810239-A-G

55143497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16810260-C-T

55143498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16810261-T-C

55145923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812260-A-G

55145966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812299-A-G

55146145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812479-G-A

55146239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812579-C-G

55146239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812579-C-T

55146297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812638-C-G

55146335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812676-G-A

55146423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812756-A-G

55146462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812804-G-A

55146462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812804-G-T

55146472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812814-T-C

55146472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812814-T-G

55146474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812816-G-A

55146474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812816-G-T

55146540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16812879-A-G

http://identifiers.org/hco/7/GRCh38#55146619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16812959-C-A

55146619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16812959-C-G

55146619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16812959-C-T

55146763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813102-C-G

55146781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813120-T-C

55146953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813275-T-C

55147003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813315-C-T

55147085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813378-A-G

55147105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813396-G-T

55147378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813633-C-G

55147534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813767-A-T

55147638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813849-T-A

55147691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813901-G-T

55147774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16813977-C-G

55147900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16814091-G-A

55147968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16814155-C-T

55148251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16814410-G-A

55148261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16814420-C-T

55148324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16814473-A-T

http://identifiers.org/hco/7/GRCh38#55148326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16814475-C-A

55148494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16814612-T-C

http://identifiers.org/hco/7/GRCh38#55148528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16815778-C-A

55148604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16815843-A-G

55148604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16815843-A-T

55148808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16815984-T-A

55148824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16816000-G-A

55149045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16816228-T-C

http://identifiers.org/hco/7/GRCh38#55149161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16816368-A-C

55150773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16816726-A-T

55150793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16816747-T-C

55150849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16816803-C-T

55151110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817036-T-A

http://identifiers.org/hco/7/GRCh38#55151148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16817080-C-A

55151148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817080-C-T

http://identifiers.org/hco/7/GRCh38#55151163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16817095-C-A

55151163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817095-C-T

55151176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817107-G-C

55151176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817107-G-T

55151284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817221-T-C

55151328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16817265-C-T

http://identifiers.org/hco/7/GRCh38#55151379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16817322-C-A

55151390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817333-T-C

55151390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817333-T-G

http://identifiers.org/hco/7/GRCh38#55151414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16817378-C-A

55151414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817378-C-T

55152220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817768-G-A

55152225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817773-G-A

55152325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817876-A-G

55152430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817977-G-A

55152430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16817977-G-T

http://identifiers.org/hco/7/GRCh38#55152466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16818032-C-A

55152466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818032-C-T

55152525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818090-G-A

55152542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16818104-T-A

55152542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16818104-T-C

55152631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16818193-A-G

55152673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818238-C-G

55152673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818238-C-T

http://identifiers.org/hco/7/GRCh38#55152717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16818276-C-A

55152717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818276-C-T

55152744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818304-T-G

55153288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818559-G-A

55153444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818682-A-G

55153444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16818682-A-T

55153849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819064-G-A

http://identifiers.org/hco/7/GRCh38#55153985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16819192-C-A

55153985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819192-C-T

55153998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819205-C-G

55153998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819205-C-T

55154170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819368-G-T

55154190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819388-A-G

55154192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819390-C-G

55154196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819393-G-C

http://identifiers.org/hco/7/GRCh38#55154274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16819461-A-C

http://identifiers.org/hco/7/GRCh38#55154296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16819483-C-A

55154346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819526-G-C

55154371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819551-G-A

http://identifiers.org/hco/7/GRCh38#55154606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16819808-A-C

55154608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819810-G-A

55154624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16819822-G-A

http://identifiers.org/hco/7/GRCh38#55154797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16819976-A-C

55154849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820026-G-A

55154849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820026-G-C

55154862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820039-G-A

55154882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820059-G-A

55154993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820229-T-A

55155112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820342-T-C

55155663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820804-G-A

http://identifiers.org/hco/7/GRCh38#55155738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16820878-C-A

55155738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16820878-C-T

55155975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821105-G-A

55155998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821128-G-C

55155998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821128-G-T

55156043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821176-T-A

55156043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821176-T-C

55156045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821178-A-G

55156045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821178-A-T

55156046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821179-A-G

55156071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821200-T-A

55156078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821207-G-A

55156078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821207-G-T

http://identifiers.org/hco/7/GRCh38#55156096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16821225-C-A

55156096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821225-C-T

55156406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821494-G-A

55156406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821494-G-T

http://identifiers.org/hco/7/GRCh38#55156431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16821503-C-A

55156431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821503-C-T

55156506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821561-G-T

55156510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821565-A-G

55156540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16821590-C-T

55156730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16821773-A-G

55156748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16821791-G-A

55156842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_retained_variant
orthologous variants: 16821885-G-A

55156842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16821885-G-T

55156856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16821898-A-G

http://identifiers.org/hco/7/GRCh38#55157008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16822045-C-A

55157053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822099-T-C

55157080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822125-G-A

55157080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822125-G-T

55157091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822136-G-A

55157214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822265-T-A

55157214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822265-T-G

55157242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822293-C-T

http://identifiers.org/hco/7/GRCh38#55157366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16822413-C-A

55157570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16822758-T-C

55157860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823021-T-G

http://identifiers.org/hco/7/GRCh38#55157879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16823043-C-A

55157916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823079-C-G

55158031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823215-C-G

55158051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823234-C-T

http://identifiers.org/hco/7/GRCh38#55158087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16823269-C-A

55158279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823399-A-G

55158335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823456-G-T

55158640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823744-A-T

55158830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16823873-G-T

55159058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824119-T-A

55159287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824251-C-G

55159292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824256-G-A

55159317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824259-C-T

55159322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824264-G-A

http://identifiers.org/hco/7/GRCh38#55159655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16824479-C-A

55159727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824550-G-A

http://identifiers.org/hco/7/GRCh38#55159876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16824695-A-C

55159879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824698-A-T

http://identifiers.org/hco/7/GRCh38#55159988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16824808-A-C

55159988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824808-A-G

55159988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824808-A-T

55159992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824813-G-A

55159992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824813-G-T

55160011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824832-A-G

55160036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824857-A-G

55160036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824857-A-T

55160037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824858-G-T

55160059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824879-T-A

55160066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824886-G-A

55160066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824886-G-C

55160066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824886-G-T

55160090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16824911-A-G

55160172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: synonymous variant
orthologous variants: 16824993-C-T

55160253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: synonymous variant
orthologous variants: 16825074-T-C

http://identifiers.org/hco/7/GRCh38#55160348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16825169-C-A

55160348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825169-C-T

55160379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825199-A-G

55160409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825229-G-A

55160409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825229-G-C

55160409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825229-G-T

http://identifiers.org/hco/7/GRCh38#55160457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16825279-A-C

55160457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825279-A-G

55160530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16825341-A-G

http://identifiers.org/hco/7/GRCh38#55160775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16827698-C-A

55160801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16827724-G-A

55160808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16827732-G-A

55161001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16827908-G-A

55161008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16827917-T-A

55161017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16827926-G-C

55161428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828057-G-T

55161664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828290-G-A

http://identifiers.org/hco/7/GRCh38#55161710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16828335-C-A

55161710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828335-C-T

55162184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828768-G-A

55162232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828813-G-A

55162232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828813-G-C

55162262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828852-T-C

55162381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16828976-A-G

55163494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16831229-C-G

55163642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16831368-C-T

55163927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16831640-A-G

55164333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16831973-T-C

55164678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16832318-G-T

55164757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16832388-G-A

55165000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16832630-C-T

55165169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16833355-A-G

http://identifiers.org/hco/7/GRCh38#55165181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16833364-C-A

55165181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16833364-C-G

55165181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16833364-C-T

55165268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16833444-A-G

55165306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: synonymous variant
orthologous variants: 16833482-C-T

55165559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16833694-T-C

55166215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834374-G-A

55166302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834423-G-A

http://identifiers.org/hco/7/GRCh38#55166313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16834434-C-A

55166313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834434-C-T

55166332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834453-T-A

55166625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834691-G-C

55166669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834739-G-C

55166669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834739-G-T

55166673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834744-G-A

55166689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834760-T-C

55166689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834760-T-G

55166754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834829-T-C

55166779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834858-A-G

55166782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834861-T-G

55166797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834876-G-T

55167804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16834980-G-A

55167881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16835061-T-C

http://identifiers.org/hco/7/GRCh38#55168100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16835271-C-A

55168100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16835271-C-T

55168115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16835286-C-T

55168269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16835425-C-T

http://identifiers.org/hco/7/GRCh38#55168736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16835628-C-A

55168736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16835628-C-T

55168868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16835754-C-T

55170846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16836821-G-A

55170846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16836821-G-T

55170883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16836865-G-C

55170922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16836887-T-A

55170922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 16836887-T-C

55171080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16837051-G-A

55171080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16837051-G-T

55171439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16837365-T-C

55171483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16837425-G-A

55171729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16837673-G-T

55172380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16838611-T-C

55172397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16838628-A-G

55172691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16839645-T-A

55172789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16839741-G-A

55172824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16839783-A-G

55172897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16839853-C-G

55172906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16839862-G-A

55172910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16839866-G-A

http://identifiers.org/hco/7/GRCh38#55173138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16840068-C-A

55173138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16840068-C-G

55173138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16840068-C-T

55174077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841348-C-G

55174077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841348-C-T

55174081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841354-G-T

55174166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841481-G-A

55174166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841481-G-T

55174393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841651-G-A

55174393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841651-G-C

55174410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841668-A-G

55174469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16841702-C-T

55174658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16842946-C-T

55174742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: synonymous variant
orthologous variants: 16843028-T-C

55174916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843427-A-G

55174916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843427-A-T

http://identifiers.org/hco/7/GRCh38#55174923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16843434-C-A

55174923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843434-C-T

55175066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843559-C-T

55175132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843619-T-C

55175172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843659-G-C

55175172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16843659-G-T

55176038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16844241-T-G

55176116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16844310-C-T

55176284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16844469-G-A

55177085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16844644-G-A

55177260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16844818-A-T

55177600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16845379-A-G

55177809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16845580-C-T

55177901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, undefined
orthologous variants: 16845670-G-A

55177963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, undefined
orthologous variants: 16845714-T-A

55180639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846269-C-G

55180639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846269-C-T

55180657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846287-T-A

55180676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846306-A-T

http://identifiers.org/hco/7/GRCh38#55180706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16846336-A-C

55180709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846339-G-A

55180709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846339-G-T

http://identifiers.org/hco/7/GRCh38#55180744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16846374-C-A

55180744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846374-C-T

55180779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846413-T-A

55180779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846413-T-C

http://identifiers.org/hco/7/GRCh38#55180782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16846416-C-A

55180782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846416-C-G

55180782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846416-C-T

55180895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846516-T-C

55180903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846525-G-A

55181000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846629-T-C

http://identifiers.org/hco/7/GRCh38#55181055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16846690-C-A

55181055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846690-C-G

55181055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846690-C-T

55181110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16846735-T-C

55181234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16846836-G-A

55181266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16846863-C-T

55181413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16847014-G-A

55181413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16847014-G-T

http://identifiers.org/hco/7/GRCh38#55181603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847331-A-C

http://identifiers.org/hco/7/GRCh38#55181647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847376-C-A

55181647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847376-C-T

55181660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847386-G-A

55181660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847386-G-T

55181673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847400-G-A

55181673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847400-G-T

http://identifiers.org/hco/7/GRCh38#55181680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847407-C-A

55181680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847407-C-G

55181680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847407-C-T

55181705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847427-G-A

55181722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847444-A-G

55181734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847456-G-A

55181734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847456-G-T

55181739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847461-G-A

55181761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847480-T-C

55181850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847566-A-G

55181853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847569-C-T

55181869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847585-C-G

55181881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847597-G-A

55181881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847597-G-T

http://identifiers.org/hco/7/GRCh38#55181904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847608-C-A

55181904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847608-C-T

55181930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847635-G-C

55181945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847638-G-A

55181945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847638-G-T

55181962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847657-G-A

55181962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847657-G-T

55181967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847662-T-A

55181967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847662-T-C

55181971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847666-G-A

55181971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847666-G-T

http://identifiers.org/hco/7/GRCh38#55181973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847668-C-A

55181973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847668-C-G

55181973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847668-C-T

55182038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847730-T-C

55182053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847745-G-A

55182053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847745-G-T

55182110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847801-G-A

55182110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847801-G-T

55182111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847802-A-G

http://identifiers.org/hco/7/GRCh38#55182128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847819-C-A

http://identifiers.org/hco/7/GRCh38#55182146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847837-C-A

http://identifiers.org/hco/7/GRCh38#55182182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847873-C-A

http://identifiers.org/hco/7/GRCh38#55182239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16847932-C-A

55182264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847957-T-C

55182308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16847986-A-G

55182354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16848034-G-A

55182354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16848034-G-T

http://identifiers.org/hco/7/GRCh38#55182394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16848067-A-C

55182394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16848067-A-G

http://identifiers.org/hco/7/GRCh38#55182418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16848090-C-A

55182418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16848090-C-T

55182429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16848109-A-G

55182479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 16848139-T-A

55182487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848147-G-T

55182551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848177-G-A

http://identifiers.org/hco/7/GRCh38#55182627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16848250-C-A

55182627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848250-C-T

http://identifiers.org/hco/7/GRCh38#55182780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16848362-A-C

55182823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848415-A-G

55182854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848446-G-A

55183154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848751-C-T

55183291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848844-T-C

55183374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16848926-T-C

55183501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849059-A-G

55183647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849211-T-C

55183733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849282-A-G

55183817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849358-C-T

55184589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849720-A-G

55184662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849790-G-A

55184666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849794-T-C

55184848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849973-C-T

55184849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849974-A-G

55184849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16849974-A-T

55184912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850038-C-T

55185011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850134-T-C

55185126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850224-A-G

http://identifiers.org/hco/7/GRCh38#55185165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16850250-A-C

55185167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850252-A-G

55186461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850417-C-T

55186479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850435-G-A

55188332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850851-C-T

55188339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16850857-C-T

55188627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16851138-G-T

55188727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16851225-G-A

http://identifiers.org/hco/7/GRCh38#55188796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#16851297-C-A

55188796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16851297-C-T

55188877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16851372-T-A

55188877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 16851372-T-C

55188899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16851396-G-A

55188899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16851396-G-T

55188925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16851413-G-T

55188942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16851426-A-G

55188954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 16851438-G-T

55189006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851493-G-A

55189006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851493-G-C

55189006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851493-G-T

55189021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851507-T-C

55189191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851591-G-A

55189201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851601-G-A

55189201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851601-G-T

55189235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851646-C-T

55189253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851661-G-T

55189292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851696-C-T

55189391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16851786-C-T

55189555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16852060-A-G

55190159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16852630-T-G

55190233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16852744-G-T

55190399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16852906-T-C

55190410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16852917-C-T

55190510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853012-T-A

55190572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853078-C-G

55190700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853207-A-G

55190740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853248-C-T

55190775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853306-A-G

55190951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853499-C-G

55191091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853634-C-T

55191281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853836-C-G

55191282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16853837-A-T

55191591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16854127-A-G

http://identifiers.org/hco/7/GRCh38#55191603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16854139-C-A

55191604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16854140-A-G

55191604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16854140-A-T

http://identifiers.org/hco/7/GRCh38#55191638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16854202-C-A

http://identifiers.org/hco/7/GRCh38#55191710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16854296-C-A

55191710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16854296-C-G

55191710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16854296-C-T

55191712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 16854298-G-C

55191856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 16854442-C-T

55191886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16854471-G-A

http://identifiers.org/hco/7/GRCh38#55192057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16854623-C-A

http://identifiers.org/hco/7/GRCh38#55192197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16854771-C-A

http://identifiers.org/hco/7/GRCh38#55192490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16855065-C-A

55192499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron variant
orthologous variants: 16855074-T-A

55192859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16855440-T-C

55192859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16855440-T-G

55192860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16855441-G-A

55192933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16855514-G-A

55192933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16855514-G-T

55193081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 16855642-A-T

55193283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16855862-A-G

55193459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16856027-C-G

55198356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16856411-T-A

55198386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16856439-T-C

55198707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16856726-A-G

55198707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16856726-A-T

55198742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16856761-C-T

http://identifiers.org/hco/7/GRCh38#55198808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16856827-A-C

55198808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16856827-A-G

55198878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16856897-G-A

55198878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16856897-G-C

55198878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16856897-G-T

http://identifiers.org/hco/7/GRCh38#55198972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16857002-A-C

55199600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16858015-G-A

http://identifiers.org/hco/7/GRCh38#55200211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16858778-A-C

55200211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16858778-A-G

55200267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16858827-A-G

http://identifiers.org/hco/7/GRCh38#55200306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16858867-C-A

55200306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16858867-C-T

http://identifiers.org/hco/7/GRCh38#55200495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859048-C-A

http://identifiers.org/hco/7/GRCh38#55200535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859085-C-A

55200535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859085-C-T

http://identifiers.org/hco/7/GRCh38#55200605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859150-C-A

55200605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859150-C-G

http://identifiers.org/hco/7/GRCh38#55200608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859153-C-A

55200608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859153-C-T

http://identifiers.org/hco/7/GRCh38#55200619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859164-C-A

55200642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859207-C-T

http://identifiers.org/hco/7/GRCh38#55200787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859348-C-A

55200787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859348-C-T

http://identifiers.org/hco/7/GRCh38#55200807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859362-C-A

55200812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859367-G-A

55200812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859367-G-T

http://identifiers.org/hco/7/GRCh38#55200828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859384-C-A

55200828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859384-C-T

55200860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859422-A-G

55200922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859483-T-G

http://identifiers.org/hco/7/GRCh38#55201039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16859598-C-A

55201039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859598-C-T

55201090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859649-C-T

55201091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859650-A-G

55201104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859663-G-A

55201150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859694-T-C

55201151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 16859695-A-G

55201223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16859767-C-T

55201377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16859911-C-G

55201377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16859911-C-T

55201515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860023-T-C

http://identifiers.org/hco/7/GRCh38#55201630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16860103-C-A

55201630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860103-C-T

http://identifiers.org/hco/7/GRCh38#55201636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16860109-C-A

55201651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860125-A-G

55201658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860132-A-T

55201670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860144-T-C

http://identifiers.org/hco/7/GRCh38#55201918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16860365-C-A

55201918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860365-C-T

55201920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860367-G-A

55201924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860405-T-C

55202300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16860723-C-T

55202511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 16860788-C-T

55202544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16860815-A-G

http://identifiers.org/hco/7/GRCh38#55202581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16860852-C-A

55202581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 16860852-C-T

http://identifiers.org/hco/7/GRCh38#55202681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16860953-A-C

55202711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 16860993-G-A

55202711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 16860993-G-T

55202798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 16861087-G-A

55205015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861269-C-G

55205090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861322-A-G

55205111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861343-G-A

55205111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861343-G-C

55205111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861343-G-T

55205167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861396-G-T

55205179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 16861408-A-G

55205359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16861597-C-T

55205557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16861795-A-G

55205599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 16861837-T-C

55205622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16861862-G-A

55205680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16861920-G-A

http://identifiers.org/hco/7/GRCh38#55205698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16861939-C-A

55205698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16861939-C-T

55205714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16861955-A-G

55205843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862105-C-G

55205977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862226-T-C

55206029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862254-T-A

55206152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862350-T-G

http://identifiers.org/hco/7/GRCh38#55206244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16862442-C-A

55206244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862442-C-T

55206296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862499-G-A

55206300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862503-T-C

55206309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862512-A-G

http://identifiers.org/hco/7/GRCh38#55206318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16862521-C-A

55206318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862521-C-T

55206321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862524-G-A

55206473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862686-A-G

55206473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862686-A-T

55206502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862715-G-A

55206502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862715-G-T

http://identifiers.org/hco/7/GRCh38#55206616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16862807-C-A

55206700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16862892-T-C

55207601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863417-A-G

55207606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863422-G-A

55207606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863422-G-T

55207646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863454-A-G

55207706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863513-C-T

55207852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863668-T-C

55207853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863669-G-A

55207903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863726-C-T

55207985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863798-G-A

55207985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863798-G-C

55207985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863798-G-T

55207986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 16863799-A-G

55208194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864010-G-A

55208196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864012-A-G

55208197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864013-C-T

http://identifiers.org/hco/7/GRCh38#55208406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864352-C-A

55208465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864406-G-T

http://identifiers.org/hco/7/GRCh38#55208531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864511-C-A

55208531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864511-C-T

55208535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864515-C-G

55208535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864515-C-T

55208544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864524-T-C

http://identifiers.org/hco/7/GRCh38#55208686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864683-C-A

55208686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864683-C-T

http://identifiers.org/hco/7/GRCh38#55208721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864718-C-A

55208721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864718-C-T

http://identifiers.org/hco/7/GRCh38#55208751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864756-C-A

http://identifiers.org/hco/7/GRCh38#55208752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864757-C-A

http://identifiers.org/hco/7/GRCh38#55208838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16864841-C-A

55208910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864896-C-G

55208910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864896-C-T

55208925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16864911-G-A

http://identifiers.org/hco/7/GRCh38#55209094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16865072-C-A

55209094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865072-C-T

55209114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865092-A-G

55209115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865093-G-A

55209244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865213-G-T

55209287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865249-G-T

55209318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865279-G-A

55209318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865279-G-T

55209779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16865772-T-C

http://identifiers.org/hco/7/GRCh38#55209954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16865973-C-A

http://identifiers.org/hco/7/GRCh38#55210053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16866036-C-A

55210095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866085-G-T

55210132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866123-A-G

55210149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866140-T-G

http://identifiers.org/hco/7/GRCh38#55210193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16866183-C-A

55210218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866212-G-T

55210259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866253-A-G

55210259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866253-A-T

http://identifiers.org/hco/7/GRCh38#55210263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16866257-A-C

55210345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866346-G-T

55210407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866412-G-T

55210580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866699-T-C

http://identifiers.org/hco/7/GRCh38#55210621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#16866734-C-A

55210621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866734-C-T

55210628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866741-A-G

55210640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866757-G-T

55210785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16866962-G-T

55210997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16867264-G-T

55211123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16867500-T-C

55211303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16867671-G-A

55211595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3236
most severe consequence: 3 prime UTR variant
orthologous variants: 16867949-C-T