87327011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122276207-A-G

87327011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122276207-A-T

http://identifiers.org/hco/16/GRCh38#87329981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122277937-C-A

87329981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122277937-C-T

http://identifiers.org/hco/16/GRCh38#87330030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122277979-C-A

87330030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122277979-C-T

87330044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122277989-A-G

87330059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278004-A-G

87330231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278129-A-G

http://identifiers.org/hco/16/GRCh38#87330249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278147-C-A

87330252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278150-G-T

87330279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278156-G-C

87330279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278156-G-T

87330286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278163-G-A

87330286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278163-G-T

http://identifiers.org/hco/16/GRCh38#87330358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278213-A-C

87330370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278231-T-A

87330370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278231-T-C

87330415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278282-C-T

87330431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278291-G-A

87330431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278291-G-T

87330434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278294-G-A

87330434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278294-G-T

87330505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278343-A-T

87330540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278378-G-A

87330540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278378-G-T

http://identifiers.org/hco/16/GRCh38#87330547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278384-C-A

87330547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278384-C-T

http://identifiers.org/hco/16/GRCh38#87330555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278392-C-A

87330555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278392-C-T

87330579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278422-G-A

87330579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278422-G-T

http://identifiers.org/hco/16/GRCh38#87330587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278430-C-A

87330587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278430-C-T

http://identifiers.org/hco/16/GRCh38#87330592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278435-C-A

87330592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278435-C-T

87330593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278436-A-G

http://identifiers.org/hco/16/GRCh38#87330608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278450-C-A

http://identifiers.org/hco/16/GRCh38#87330623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278465-C-A

87330656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278479-A-G

87330662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278484-G-T

87330724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278532-T-C

87330746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278554-C-T

http://identifiers.org/hco/16/GRCh38#87331033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278743-A-C

87331033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278743-A-G

87331033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278743-A-T

http://identifiers.org/hco/16/GRCh38#87331057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122278767-C-A

87331057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278767-C-G

87331057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278767-C-T

87331149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278863-G-A

87331149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278863-G-T

87331277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278952-G-C

87331277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 122278952-G-T

87331354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 122279028-G-A

87331354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122279028-G-C

87331354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 122279028-G-T

87331471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 122279145-G-A

87331514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 122279188-A-G

87333264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122280099-C-T

87333279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122280119-C-T

87333891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 122280849-C-T

87333903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 122280861-G-C

87334090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 122281015-C-T

http://identifiers.org/hco/16/GRCh38#87334096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122281023-C-A

87334096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 122281023-C-T

87334109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 122281028-G-A

87334109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 122281028-G-C

87334109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 122281028-G-T

87334116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 122281035-G-A

87334326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281239-G-T

http://identifiers.org/hco/16/GRCh38#87334573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122281455-C-A

87334755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281587-C-T

87334808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281622-T-C

87334808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281622-T-G

http://identifiers.org/hco/16/GRCh38#87335252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122281895-A-C

87335252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281895-A-G

87335252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281895-A-T

87335255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281901-T-G

http://identifiers.org/hco/16/GRCh38#87335277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122281921-C-A

87335277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122281921-C-T

87335385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 122282026-G-A

87335463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 122282106-G-T

87335525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282181-G-A

87335525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282181-G-C

87335525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282181-G-T

87335562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282247-A-G

87335562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282247-A-T

87335675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282402-G-A

87336004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282812-G-A

87336004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282812-G-C

http://identifiers.org/hco/16/GRCh38#87336010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122282818-A-C

87336088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282910-G-A

87336088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282910-G-C

87336088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122282910-G-T

87336208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 122283034-G-A

87336208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122283034-G-C

87336208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 122283034-G-T

http://identifiers.org/hco/16/GRCh38#87336226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122283052-C-A

87336226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 122283052-C-T

http://identifiers.org/hco/16/GRCh38#87336295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122283118-A-C

87336295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283118-A-G

http://identifiers.org/hco/16/GRCh38#87336319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122283138-C-A

87336340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283157-G-T

87336382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283179-G-C

87336382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283179-G-T

87336398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283195-G-A

87336398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283195-G-C

87336401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283198-G-T

http://identifiers.org/hco/16/GRCh38#87336452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122283231-C-A

87336452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283231-C-T

http://identifiers.org/hco/16/GRCh38#87336544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122283338-C-A

87336544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122283338-C-T

87342391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122285288-T-G

87342417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122285314-A-G

87342574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122285469-C-T

http://identifiers.org/hco/16/GRCh38#87342601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122285490-C-A

87342668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122285547-A-T

87342814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122285658-C-G

87343325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286331-A-G

87343413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286413-C-G

87343413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286413-C-T

http://identifiers.org/hco/16/GRCh38#87343446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122286445-A-C

87343446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286445-A-G

87343454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286453-C-T

87343459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286463-G-A

87343459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286463-G-C

87343459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286463-G-T

87343464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286468-G-A

87343464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286468-G-T

http://identifiers.org/hco/16/GRCh38#87343529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122286542-C-A

87343529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286542-C-G

87343529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286542-C-T

87343536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286550-G-C

87343536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286550-G-T

http://identifiers.org/hco/16/GRCh38#87343538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122286552-C-A

87343538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286552-C-G

87343538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 122286552-C-T

87343694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 122286758-T-C

http://identifiers.org/hco/16/GRCh38#87346963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122286979-A-C

87347024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122287040-G-A

87347024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122287040-G-T

87347157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122287110-G-A

87347269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122287220-A-G

87347300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122287248-C-T

http://identifiers.org/hco/16/GRCh38#87358292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122291259-C-A

87358344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291297-G-A

87358344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291297-G-T

87358348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291301-T-C

87358364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291319-G-C

87358502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122291468-A-G

87358818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291673-G-C

http://identifiers.org/hco/16/GRCh38#87358915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122291763-C-A

87358915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291763-C-T

87358958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291796-G-C

87358971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122291809-G-A

87359321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122292080-C-T

http://identifiers.org/hco/16/GRCh38#87359467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122292196-C-A

87359467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122292196-C-T

87359486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122292214-G-A

87359524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122292249-T-C

87359632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122292333-C-T

87360227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122292941-T-A

87360323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122293042-G-A

87360383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293102-T-C

87360383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293102-T-G

87360404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293120-A-G

87360407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293128-T-G

87360450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293161-G-A

87360450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293161-G-C

87360450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293161-G-T

87360613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122293284-T-C

http://identifiers.org/hco/16/GRCh38#87360620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122293291-A-C

87363896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122295166-C-G

87364050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122295304-T-A

87364162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122295412-C-G

87368331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122297288-T-C

87368464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122297430-G-C

87368518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122297479-G-A

http://identifiers.org/hco/16/GRCh38#87375857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122302034-A-C

87375922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122302098-C-G

87375922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122302098-C-T

87375960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122302118-G-C

87380895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122303709-G-T

http://identifiers.org/hco/16/GRCh38#87382055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122304686-C-A

87382055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122304686-C-T

87383394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122305186-C-G

87383394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122305186-C-T

http://identifiers.org/hco/16/GRCh38#87383398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122305190-C-A

87383398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122305190-C-T

87383444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122305236-G-A

87383444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122305236-G-C

87383444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122305236-G-T

87383448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122305240-G-A

87383448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122305240-G-T

http://identifiers.org/hco/16/GRCh38#87383502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122305294-C-A

87383502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122305294-C-T

87383724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122305474-A-G

87383774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122305573-T-C

87383781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122305580-A-G

http://identifiers.org/hco/16/GRCh38#87383787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122305601-C-A

87383787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122305601-C-T

http://identifiers.org/hco/16/GRCh38#87383854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122305670-A-C

87383854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122305670-A-G

http://identifiers.org/hco/16/GRCh38#87383936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122305820-C-A

http://identifiers.org/hco/16/GRCh38#87383949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122305870-C-A

87383949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122305870-C-T

87384016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122305960-T-A

87384016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122305960-T-C

87384016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122305960-T-G

87384129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122306076-G-T

87386326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122310621-G-A

87386326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122310621-G-T

87386329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122310624-G-T

87389211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313333-T-C

87389236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313358-A-G

87389237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313371-T-G

87389385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313492-A-G

87389478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313561-A-G

87389478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313561-A-T

87389498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16510
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122313579-C-T