http://identifiers.org/hco/1/GRCh38#224434677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181039440-C-A

224434677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181039440-C-T

http://identifiers.org/hco/1/GRCh38#224434724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181039474-C-A

224434724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 181039474-C-T

224434928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039687-A-G

http://identifiers.org/hco/1/GRCh38#224434936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181039695-C-A

224435025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039769-G-T

224435068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039817-G-A

224435068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039817-G-T

224435075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039824-G-A

224435106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 181039853-G-A

224435106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039853-G-C

224435106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039853-G-T

224435117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039872-T-C

224435177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181039929-A-G

224435203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181039948-G-A

224435203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181039948-G-C

224435203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181039948-G-T

224435213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181039958-G-T

224435252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181039996-A-G

224435448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181040214-A-G

224435774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 181040485-G-A

224435823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 181040529-A-T

http://identifiers.org/hco/1/GRCh38#224436754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181041443-C-A

224436754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181041443-C-T

http://identifiers.org/hco/1/GRCh38#224436766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181041455-C-A

224436772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181041461-G-T

224436788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181041477-T-A

http://identifiers.org/hco/1/GRCh38#224436891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181041688-C-A

224436893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 181041690-G-A

224436893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 181041690-G-T

224436939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 181041797-C-T

224436993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 181041952-A-G

224437046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181041996-T-C

224437102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181042054-G-C

224437102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181042054-G-T

224437768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181042710-A-G

224437768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181042710-A-T

224438479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181043419-G-C

224439028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181043935-T-C

224439132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044047-G-T

224439283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044145-C-T

224439384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044227-T-G

224439403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044248-A-G

224439415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044254-A-G

http://identifiers.org/hco/1/GRCh38#224439466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181044277-C-A

224439466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044277-C-G

224439466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044277-C-T

224441217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181044974-G-A

224441547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181045339-T-C

http://identifiers.org/hco/1/GRCh38#224441586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181045380-C-A

224441680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181045445-T-C

224442682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047081-T-A

224442682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047081-T-C

224442851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047242-C-G

224443162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047553-A-G

224443241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047622-G-T

http://identifiers.org/hco/1/GRCh38#224443309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181047701-C-A

224443412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047784-C-T

224443594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181047961-C-G

224446569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181052729-G-A

224446727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181052857-G-A

224446759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181052889-T-G

224446764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181052894-C-G

224446764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181052894-C-T

224446882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181053005-C-T

224447594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181053166-G-A

224448345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181054286-G-A

224448390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181054344-A-G

224448456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181054393-C-G

224448543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181054477-T-G

http://identifiers.org/hco/1/GRCh38#224448581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181054514-C-A

224450130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055323-A-G

224450130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055323-A-T

224450343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055498-G-A

224450350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055505-A-G

224450371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055526-A-G

224450616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055755-A-G

224450625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055764-C-G

224450625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055764-C-T

224450680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055818-A-G

224450680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181055818-A-T

224451249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181056355-G-A

224451321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181056423-A-G

http://identifiers.org/hco/1/GRCh38#224451710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181056772-A-C

224451748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181056810-G-T

224451822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181056886-G-A

224453831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181057708-C-G

224453831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181057708-C-T

224453931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181057801-T-C

http://identifiers.org/hco/1/GRCh38#224454157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181057942-C-A

224454186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181057971-G-A

224454186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181057971-G-T

224454188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181057973-A-G

http://identifiers.org/hco/1/GRCh38#224454381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181058159-A-C

224454381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181058159-A-G

224454484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181058262-G-A

224454806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181058603-G-A

224456063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059383-G-T

224456126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059450-G-A

224456174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059479-T-C

224456267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059562-C-T

224456280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059564-G-A

224456283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059567-C-G

224456283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059567-C-T

224456341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181059624-A-G

http://identifiers.org/hco/1/GRCh38#224457376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181060184-A-C

http://identifiers.org/hco/1/GRCh38#224457416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181060217-C-A

http://identifiers.org/hco/1/GRCh38#224457417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181060218-C-A

224457433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181060233-T-C

224457553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181060328-C-T

http://identifiers.org/hco/1/GRCh38#224457626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181060399-C-A

224457626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181060399-C-T

224458157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181061494-G-T

224458587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181061606-A-G

224458631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181061644-T-C

224458668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181061670-G-A

224458969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181061939-T-C

http://identifiers.org/hco/1/GRCh38#224459250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181062168-A-C

224459250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062168-A-G

224459374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062293-T-G

224459420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062329-G-A

224459420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062329-G-C

224459544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062435-G-A

224459544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062435-G-C

224459710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062570-G-C

224459783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062641-G-T

224459850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062705-G-A

224459871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062728-T-G

224459879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181062736-C-G

224485779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181065908-T-C

224485950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181066039-G-A

224485951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181066040-G-A

224486037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181066115-C-T

224486073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181066152-G-T

224486670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181066765-G-T

224487084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181067075-G-C

224487084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181067075-G-T

224487252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181067217-C-T

224487277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181067247-A-G

224487429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181067397-A-G

224487430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181067398-T-C

224490392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181069977-G-A

224490443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181070022-A-T

224490459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181070043-G-T

224490491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181070072-T-C

224490571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181070153-T-G

224493894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181077307-C-T

224494964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075986-A-G

224495034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075920-A-G

224495036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075918-G-T

224495258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075733-A-G

224495388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075618-T-A

224495435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075576-C-T

224497802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181075401-G-A

http://identifiers.org/hco/1/GRCh38#224497951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181075280-A-C

224498550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074800-G-A

224498647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074671-A-T

224498675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074647-C-T

224498768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074577-G-A

224498768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074577-G-C

224498833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074501-G-A

224498833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181074501-G-T

224501898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181083486-A-T

224501947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181083530-G-A

224501947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181083530-G-C

224502231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181083800-G-A

224502433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181083967-G-A

224502625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181084118-G-A

224502995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181084452-T-G

http://identifiers.org/hco/1/GRCh38#224503066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181084500-C-A

224503520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181084880-C-T

224503560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181084886-C-T

224503732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181085029-C-T

224503746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181085042-G-A

224504124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181085246-T-C

224504161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181085276-C-T

224504406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181085510-G-A

224504619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181085813-T-A

224504619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181085813-T-G

224505273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086342-G-A

224505273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086342-G-T

224505373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086441-T-A

224505524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086541-A-G

224505676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086673-G-C

224505682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086679-G-C

224505683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086680-G-A

224505683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086680-G-T

224505736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086734-C-T

224506008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086990-C-T

http://identifiers.org/hco/1/GRCh38#224506009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181086991-C-A

224506012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181086994-C-T

224506093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087065-A-G

224506127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087099-T-C

224506136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087108-T-C

http://identifiers.org/hco/1/GRCh38#224506222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181087188-C-A

224506236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087201-A-T

224506415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087324-C-T

224506452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087361-C-T

224506720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181087578-C-T

224508344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090000-C-T

224508374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090030-G-A

224508451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090280-T-C

224508627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090447-T-C

http://identifiers.org/hco/1/GRCh38#224508660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181090483-A-C

224508660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090483-A-G

224508663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090486-T-G

224508768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181090557-A-G

http://identifiers.org/hco/1/GRCh38#224508838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181090603-A-C

224510731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181098492-G-A

224510780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181098532-G-A

224510780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181098532-G-T

224510886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181098612-T-C

224511071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181098785-G-C

224513649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181100392-C-T

224513672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181100411-T-C

224513809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 181100557-A-G

http://identifiers.org/hco/1/GRCh38#224513813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181100561-C-A

224513813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 181100561-C-T

http://identifiers.org/hco/1/GRCh38#224513815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181100563-A-C

224513815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 181100563-A-G

224513818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 181100566-G-A

224513861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181100596-G-A

224513861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181100596-G-C

224516510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181113241-C-T

224516613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181113333-T-A

224516632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181113352-G-A

224517193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181113848-G-T

224517266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181113926-T-A

224517389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181114052-G-A

224520720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115191-G-A

224520758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115229-T-A

224520791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115253-G-A

http://identifiers.org/hco/1/GRCh38#224520861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181115318-C-A

224520918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115383-T-C

224521158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181115621-T-G

224521310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181115733-A-G

224521310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181115733-A-T

224521330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181115753-A-G

http://identifiers.org/hco/1/GRCh38#224521355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181115765-C-A

224521355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181115765-C-G

224521355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181115765-C-T

http://identifiers.org/hco/1/GRCh38#224521456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181115865-C-A

224521597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115927-T-C

224521601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115928-C-G

224521601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181115928-C-T

224521703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181116018-A-G

224521962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181116545-G-A

224522051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181116639-T-C

224522336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181116915-A-T

224522360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181116939-A-G

224522404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181116983-T-A

224522485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181117067-G-A

224525867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181117963-C-G

224526122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181118209-C-T

224526127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181118216-T-C

224527516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181118984-A-G

http://identifiers.org/hco/1/GRCh38#224527700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181119167-C-A

224527700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119167-C-T

224528930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181119569-G-C

224529068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119693-C-T

224529069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119694-A-G

224529081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119707-G-A

http://identifiers.org/hco/1/GRCh38#224529091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181119713-C-A

224529091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119713-C-G

http://identifiers.org/hco/1/GRCh38#224529115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181119737-C-A

224529115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119737-C-T

224529116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119738-A-G

224529122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181119743-A-G

224529129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181119753-G-A

224529129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181119753-G-T

224529130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181119754-G-A

224529130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181119754-G-T

224529252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181119849-G-T

224529401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181119931-A-G

224529425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119946-G-T

224529465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181119986-C-T

224529480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120005-G-T

224529486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120011-A-T

224529528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120052-A-G

224529541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120063-A-T

224529604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120124-G-A

224529707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120641-C-T

224529829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120754-C-G

224529829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120754-C-T

224529830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181120755-G-A

224530212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181121369-G-T

http://identifiers.org/hco/1/GRCh38#224530329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181121489-C-A

224532990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181123781-A-T

224534564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125034-G-A

224534571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125041-G-A

224534706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125177-T-C

224534836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125277-A-G

http://identifiers.org/hco/1/GRCh38#224534889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181125331-C-A

224535165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125574-T-C

224535219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125625-G-A

224535243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125655-C-T

224535311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181125738-G-A

224539452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181126660-C-T

224539673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181126846-C-T

224539805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181126913-G-T

224540603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181127717-G-A

224541087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181129352-G-A

224541087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181129352-G-T

224541222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181129481-G-C

224541384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181129685-G-A

224541700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181129989-C-T

224541745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181130076-A-G

http://identifiers.org/hco/1/GRCh38#224541879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181130199-C-A

224542173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181130504-A-G

224542177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181130508-A-T

224542341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181130666-C-G

224542493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181130814-C-T

224542730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131094-A-G

224542852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181131192-A-G

224542916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181131256-C-T

224546788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131412-A-G

http://identifiers.org/hco/1/GRCh38#224546851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181131450-C-A

224546851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181131450-C-T

http://identifiers.org/hco/1/GRCh38#224546952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181131536-C-A

224546952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131536-C-G

http://identifiers.org/hco/1/GRCh38#224546965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181131549-C-A

224546966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131550-A-G

224546977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131561-A-G

224546987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131571-T-C

224547105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181131686-T-C

224553408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181141002-G-A

224553592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181141109-T-G

224555174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181142123-G-A

224555174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181142123-G-T

224555193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181142142-C-G

224555218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181142167-A-T

224555837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181142912-C-T

224556031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143084-C-T

224556198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143320-C-T

224556201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143323-G-T

224556224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143424-G-T

224556228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143428-A-G

224556228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143428-A-T

224556235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181143436-A-T

224558261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181144415-G-A

224558811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181144707-T-C

224558948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181144837-G-A

224559208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181145091-G-A

224560091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181145798-G-A

224560092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181145799-T-C

224560300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181146035-A-G

224560411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181146124-C-G

http://identifiers.org/hco/1/GRCh38#224560547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181146249-C-A

224560826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181146396-A-G

224561378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181146944-T-C

224561427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181146999-C-G

224561560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147118-G-A

224561564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147122-G-A

224561564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147122-G-C

224561801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147303-C-T

224561900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147371-G-A

224561900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147371-G-C

224561998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147465-G-A

224562089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181147556-T-C

224563280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148389-T-C

224563322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148432-G-A

224563457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148512-C-G

224563457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148512-C-T

http://identifiers.org/hco/1/GRCh38#224563506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181148565-C-A

224563506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148565-C-T

224563524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148588-G-T

http://identifiers.org/hco/1/GRCh38#224563602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181148649-A-C

224563602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148649-A-G

224563614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148652-C-T

224563617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181148655-T-C

http://identifiers.org/hco/1/GRCh38#224563976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181149004-A-C

224563976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181149004-A-G

224564132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181149137-C-G

224564479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181150728-G-A

224564769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151026-G-A

http://identifiers.org/hco/1/GRCh38#224564882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181151140-C-A

224564882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151140-C-G

224564996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151227-T-C

224565152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151376-A-G

224565234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151438-T-C

224565234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151438-T-G

224565342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151527-G-T

224565356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181151541-G-A

224565356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181151541-G-T

224565406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181151590-G-T

http://identifiers.org/hco/1/GRCh38#224565431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181151652-C-A

224565678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181151865-A-G

224565785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181151948-C-T

http://identifiers.org/hco/1/GRCh38#224565814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181151967-C-A

224565879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181151995-A-G

http://identifiers.org/hco/1/GRCh38#224565949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181152070-C-A

224565959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152080-T-C

224565996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152118-G-A

224565996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152118-G-T

224566278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152354-G-A

224566278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152354-G-T

224566306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152381-G-A

224566306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152381-G-T

http://identifiers.org/hco/1/GRCh38#224567790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181152666-C-A

224567790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181152666-C-T

224581476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181157875-T-C

224581630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181158180-A-G

224581791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181158336-G-A

224582206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181158724-C-T

224582297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181158816-G-C

224582881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159175-A-G

224583104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159410-C-T

224583286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159920-G-A

224583286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159920-G-T

224583287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159921-G-A

224583291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159925-G-A

224583291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159925-G-T

224583388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159999-A-G

224583388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181159999-A-T

224583546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181160044-A-G

http://identifiers.org/hco/1/GRCh38#224583564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181160060-A-C

224583564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181160060-A-G

224583778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181160248-A-G

224583796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181160266-G-A

224584096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181160510-A-G

http://identifiers.org/hco/1/GRCh38#224585057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181164739-C-A

224585057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181164739-C-T

224585813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181165636-T-G

224585844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181165666-A-G

224585928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181165735-A-G

224586115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181165951-G-T

224586126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181165961-T-C

224586677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166101-G-A

224586841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166254-G-A

http://identifiers.org/hco/1/GRCh38#224587054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181166433-C-A

224587054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166433-C-T

224587063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166442-G-A

224587106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166465-G-A

224587117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166476-G-A

224587117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166476-G-T

224587238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166596-A-G

224587239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166597-G-T

http://identifiers.org/hco/1/GRCh38#224587243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181166601-C-A

224587243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166601-C-T

http://identifiers.org/hco/1/GRCh38#224587262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181166620-C-A

224587262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166620-C-T

224587324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166678-G-A

224587334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166695-A-G

http://identifiers.org/hco/1/GRCh38#224587343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181166704-C-A

224587350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166711-G-T

224587383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166734-G-T

224587404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181166755-T-C

224587478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181166788-C-T

224588005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181167010-G-A

224588299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181168235-T-C

224588342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181168282-G-A

224588342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181168282-G-T

224588417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181168356-G-A

224588446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181168384-T-C

224588513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181168433-T-A

http://identifiers.org/hco/1/GRCh38#224588676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181168622-C-A

224588870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181168781-G-A

224589000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181168867-G-T

224590630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181169797-T-C

224590658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181169828-G-T

224590875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181169980-G-A

224591155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181170207-A-T

224591286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181170328-A-G

224591476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181170499-G-C

http://identifiers.org/hco/1/GRCh38#224591580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181170601-A-C

224591875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181170865-G-A

http://identifiers.org/hco/1/GRCh38#224592300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181171197-A-C

224592327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181171225-C-T

224592402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181171275-C-T

224602460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181177851-T-C

224602539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181177779-G-A

224602638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181177701-G-A

http://identifiers.org/hco/1/GRCh38#224602790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181177552-A-C

224604585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181176184-G-T

224607080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181175858-G-A

224607928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181175744-T-A

http://identifiers.org/hco/1/GRCh38#224609376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181175455-A-C

224609384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181175448-C-T

224609667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181175211-G-T

224611237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181174266-G-C

224611685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181173475-A-G

http://identifiers.org/hco/1/GRCh38#224612004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181173105-A-C

224612065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181173042-T-C

224612378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181172793-C-T

http://identifiers.org/hco/1/GRCh38#224615279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181179320-A-C

224615280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181179321-G-T

224615292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181179333-G-T

http://identifiers.org/hco/1/GRCh38#224615360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181179396-C-A

224615429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 181179451-T-A

224615429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 181179451-T-G

224615524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181179516-G-A

224615524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181179516-G-T

224615663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181179664-G-A

224615663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181179664-G-T

224615746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181179745-G-A

224615834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181179833-T-G

224615975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181179951-G-A

224615975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181179951-G-T

http://identifiers.org/hco/1/GRCh38#224615998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181179961-C-A

http://identifiers.org/hco/1/GRCh38#224616135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180066-C-A

224616135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180066-C-G

224616135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180066-C-T

224616139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180070-C-T

http://identifiers.org/hco/1/GRCh38#224616183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180081-C-A

224616183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180081-C-G

224616183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180081-C-T

http://identifiers.org/hco/1/GRCh38#224616231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180129-C-A

224616231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181180129-C-G

224616231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181180129-C-T

224616311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181180196-G-A

224616311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181180196-G-T

http://identifiers.org/hco/1/GRCh38#224616318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180203-C-A

224616318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180203-C-T

http://identifiers.org/hco/1/GRCh38#224616345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180224-C-A

224616345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180224-C-G

224616345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180224-C-T

224616364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180243-T-A

224616364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180243-T-C

224616364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180243-T-G

224616381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180270-T-C

224616381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180270-T-G

224616455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180343-T-A

224616455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180343-T-C

224616488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180373-G-A

224616488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180373-G-C

224616488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180373-G-T

http://identifiers.org/hco/1/GRCh38#224616502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180387-C-A

224616502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180387-C-T

http://identifiers.org/hco/1/GRCh38#224616508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181180393-C-A

224616508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180393-C-T

224616618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180502-T-C

224616706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180564-G-A

224616706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180564-G-C

224616781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180617-C-T

224616997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180816-G-A

224616997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180816-G-T

224617067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181180890-G-C

224617235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181181051-A-G

http://identifiers.org/hco/1/GRCh38#224617319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181181155-C-A

http://identifiers.org/hco/1/GRCh38#224617376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181181232-C-A

224617468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181181342-A-G

224618047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181181760-C-T

224618518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182192-A-G

224618601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182274-T-C

http://identifiers.org/hco/1/GRCh38#224618752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181182386-A-C

224618848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182470-T-C

224619100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182850-G-A

224619100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182850-G-T

224619123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182872-C-G

224619165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182912-G-A

224619211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181182988-A-G

224619255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181183036-G-T

224619308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181183090-T-A

224619351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181183125-G-A

224619655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181183387-A-G

224619695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181183424-T-C

224620028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181183760-G-A

224620288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181184085-G-T

224620592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181184448-T-C

224620986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181184794-G-A

224620999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181184806-T-C

http://identifiers.org/hco/1/GRCh38#224621163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181185401-C-A

224621651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181185904-C-T

224622452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181186250-G-C

224622537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181186301-T-C

224622952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181186683-T-C

224623098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181186828-C-G

224623983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181188313-A-G

224624084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181188386-C-T

224624100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181188400-T-C

224624277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181188577-C-T

224624402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181188704-T-G

224624626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189184-A-G

224624669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189225-C-T

224624699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189256-A-G

224624897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189438-A-G

224624926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189468-A-G

224624942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189484-C-G

224624959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189502-G-A

http://identifiers.org/hco/1/GRCh38#224625107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181189633-A-C

224625107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189633-A-G

224625195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189727-C-T

224625298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189790-C-T

224625324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181189816-C-T

224625899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181190532-G-A

224625977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181190603-C-G

224625977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181190603-C-T

224626565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181191631-T-C

224626668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181191730-G-A

224626842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181191879-T-C

224626898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181191937-A-G

224626917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181191954-A-G

224627049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181192144-A-G

http://identifiers.org/hco/1/GRCh38#224627954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181193393-A-C

224628015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181193453-C-T

http://identifiers.org/hco/1/GRCh38#224628305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181193734-A-C

224628337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181193761-T-G

224628379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181193801-C-T

224628444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181193844-C-G

224629635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181194751-G-A

224630481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181195771-A-G

224630482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181195772-G-A

224631395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181196568-C-G

224631769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181196927-C-G

224632285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181197397-G-C

224632482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181197585-T-G

224632600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181197864-A-G

224632747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181198045-C-T

224632925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181198221-C-T

224633018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181198317-C-G

224633609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181198614-A-T

224633685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181198672-G-T

224633686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181198673-G-T

224633750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181198715-G-T

224634040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181199000-T-C

http://identifiers.org/hco/1/GRCh38#224634395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181199298-C-A

224636844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181201860-A-T

224637452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202418-T-G

224637509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202488-G-T

224637747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202692-C-T

224637759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202703-C-T

224637808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202743-C-T

224638043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202926-G-A

224638091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181202962-C-T

http://identifiers.org/hco/1/GRCh38#224638155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181203004-C-A

224638189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181203038-T-C

224638218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181203067-G-A

224638376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181203173-G-A

224638583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181203282-G-T

224638593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181203292-T-C

224640952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181204568-T-A

224640972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181204592-G-C

224640997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181204617-G-A

224641062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181204825-C-T

224641156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181204940-C-T

224641374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181205114-C-T

224641406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181205144-C-T

224644615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181207317-A-G

224644631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181207331-C-T

http://identifiers.org/hco/1/GRCh38#224645230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181207718-C-A

224645231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181207719-C-T

224645444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181207904-G-A

224645647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181209145-G-T

224645903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181209395-A-G

224646042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181209535-C-G

224647502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181209920-G-T

224647545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181209963-T-C

224647563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181209981-C-T

http://identifiers.org/hco/1/GRCh38#224647590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181210010-C-A

224648063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181210433-T-G

http://identifiers.org/hco/1/GRCh38#224648793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181211204-A-C

224648869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181211273-C-G

224649267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181211651-T-G

http://identifiers.org/hco/1/GRCh38#224649752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181212119-C-A

224649850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181212207-G-T

224649856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181212213-C-T

224651026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181215245-G-A

224651026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181215245-G-C

224651035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181215254-T-G

http://identifiers.org/hco/1/GRCh38#224651185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181215396-C-A

224651482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181215772-T-C

224651509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181215796-T-C

224651509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181215796-T-G

224651737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181216414-T-A

224651828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181216504-G-T

224651922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181216600-C-T

224652212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181216868-C-T

224652426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181217035-T-C

http://identifiers.org/hco/1/GRCh38#224652487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181217090-A-C

224652487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181217090-A-T

224652594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181217189-C-T

224652610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181217207-G-T

224670367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181223428-C-T

224670399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181223458-C-T

224671541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181223886-A-T

224671557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181223903-C-T

224672247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181224382-C-T

224672422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181224555-C-G

224672741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181224891-A-G

224672930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181225275-T-C

224673342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181225570-A-G

224673352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181225580-T-C

224673373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181225602-G-C

224673977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227064-A-G

224674001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227086-C-T

224674208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227270-A-G

224674268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181227303-G-T

224674324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227327-G-C

224674324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227327-G-T

224674550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227491-A-G

224674569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227510-C-T

224674622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181227569-G-T

224674996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181228515-G-A

224675063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181228565-C-T

224675077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181228579-C-G

224675077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181228579-C-T

224675106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181228605-T-C

224675579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181229093-G-C

http://identifiers.org/hco/1/GRCh38#224675822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181229332-C-A

http://identifiers.org/hco/1/GRCh38#224676124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181229592-A-C

http://identifiers.org/hco/1/GRCh38#224676333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181229787-C-A

224676337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181229791-G-A

224679455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181232279-G-A

224679707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181232486-G-T

224679713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181232492-T-C

224679827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181232596-T-C

224679852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181232621-G-A

http://identifiers.org/hco/1/GRCh38#224680164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181233288-C-A

224680164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233288-C-T

224680452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233557-T-C

224680498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233596-A-G

224680824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233894-C-G

224680824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233894-C-T

http://identifiers.org/hco/1/GRCh38#224680846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181233919-C-A

224680847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233920-T-C

224680877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233951-G-T

http://identifiers.org/hco/1/GRCh38#224680896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181233971-C-A

224680896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233971-C-T

224680907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233977-G-A

224680907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181233977-G-C

224680934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234008-T-C

224680934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234008-T-G

224680944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234018-G-C

224680944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234018-G-T

224680972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 181234046-T-G

224681017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 181234091-T-C

224681055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234128-G-T

http://identifiers.org/hco/1/GRCh38#224681131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181234193-C-A

224681131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234193-C-T

224681171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234232-G-A

224681317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234374-A-G

224681406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234458-C-T

224681508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234564-A-G

224682392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234686-T-C

224682504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234809-A-G

224682605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181234911-A-G

http://identifiers.org/hco/1/GRCh38#224682916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181235173-C-A

224683092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235362-C-T

224683381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235516-T-C

224683722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235720-T-C

224683847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235820-C-T

224683848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235821-G-A

224683848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235821-G-T

224684008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181235973-G-A

224684308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181236260-G-C

224684496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181236417-G-A

http://identifiers.org/hco/1/GRCh38#224684519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181236434-A-C

224684572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181236473-T-C

224684660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237075-C-T

224684750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237150-G-A

224684782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237182-G-A

224684782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237182-G-T

224684798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 181237196-G-T

224684900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237279-A-G

224685035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237377-A-G

224685043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237385-G-A

224685043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237385-G-C

224685267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237611-T-C

224685374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237632-T-C

224685555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237812-G-A

http://identifiers.org/hco/1/GRCh38#224685561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181237818-C-A

224685679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181237942-T-C

224685894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181238142-T-C

224685935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181238183-A-G

224686559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181238268-G-A

http://identifiers.org/hco/1/GRCh38#224686586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181238284-A-C

224686777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181238456-G-T

224687040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181238730-A-G

224687113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181238808-G-T

224688344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181239157-T-A

224688383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181239197-C-T

224688488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181239288-C-T

224688969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

224689562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181240687-G-A

224689878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181240997-C-G

224690709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241521-A-G

224690713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241525-G-A

224690713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241525-G-C

224690755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241568-A-G

224690835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241633-G-T

224691124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241878-T-C

224691184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181241935-A-G

224691392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181242183-G-A

224691653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181242434-T-C

224692492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244025-A-G

224692533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244066-G-A

224692533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244066-G-T

224692925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244424-T-A

224693097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244570-T-C

224693217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244686-A-G

224693413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244902-T-G

224693443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181244934-G-T

224693617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245086-G-A

224693862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245365-T-C

224693926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245432-G-A

224693933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245438-C-T

224694018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245524-G-C

224694039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245545-T-C

224694117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245622-G-A

224694213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245725-C-T

224694304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181245815-A-G

http://identifiers.org/hco/1/GRCh38#224696896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181246506-C-A

224696896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181246506-C-T

224697085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181246705-A-G

224697169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181246787-C-T

224697170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181246788-G-A

224697214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181246833-T-C

224697605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181247236-G-A

224697605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181247236-G-C

224697980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181247601-C-T

224698128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181247748-T-A

224698240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181247860-A-G

224698313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181247933-T-C

224698377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181247994-A-G

224698413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181248030-T-C

http://identifiers.org/hco/1/GRCh38#224698489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181248105-C-A

224699063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181249133-G-A

224699221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181249261-T-C

http://identifiers.org/hco/1/GRCh38#224699251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181249287-C-A

224700062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181249454-G-A

224700062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181249454-G-C

224700385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181249777-G-C

224700527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181249913-T-C

224700881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181250393-C-T

224701154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181250633-G-C

224701192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181250663-G-A

224701225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181250689-G-A

224701258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181250720-T-C

224701392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181250857-C-T

224701399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181250864-G-A

224701557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181251000-T-C

http://identifiers.org/hco/1/GRCh38#224701615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181251036-C-A

224701615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181251036-C-T

224701745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181251155-A-G

224701803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181251213-A-G

224702217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181252679-A-G

224702265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181252723-C-T

224702579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181253160-G-A

224702580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181253161-C-T

224702844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181253465-C-G

224703071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181253744-G-A

224703199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181253839-C-T

224703295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181253924-G-A

224703518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181254146-C-G

224703797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181254381-C-T

224704124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181254705-G-A

224704145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181254728-T-C

224704151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181254734-C-G

224705234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181255961-G-A

224705381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256118-C-G

224705381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256118-C-T

224705562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256273-G-A

224705632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256344-C-T

224705666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256388-C-G

224705688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256433-G-T

224705691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256436-T-C

224705714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181256459-G-C

http://identifiers.org/hco/1/GRCh38#224705908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181256586-C-A

224707665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181257166-T-G

224707977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181257461-T-G

http://identifiers.org/hco/1/GRCh38#224708535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181257990-A-C

224708682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258098-C-T

224708800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258169-C-T

224710603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258422-T-C

224710623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258438-C-T

224710663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258478-C-T

224710734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258531-A-G

224710863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258737-T-A

224710893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258767-G-A

224710893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258767-G-C

224710894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181258768-C-T

224710937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 181258808-T-G

224712099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181260237-C-T

224712424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181260534-C-T

224712942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261069-A-G

224713096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261224-T-A

224713168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261304-T-C

224713409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261556-C-T

224713424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261571-G-A

224713569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261701-A-G

224713715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261831-C-G

224713744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181261844-T-C

http://identifiers.org/hco/1/GRCh38#224714058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181262009-A-C

http://identifiers.org/hco/1/GRCh38#224714062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181262013-C-A

224714157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262150-T-G

224714192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262185-G-A

224714362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262332-A-G

http://identifiers.org/hco/1/GRCh38#224714379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181262348-A-C

224714396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262365-A-T

224714590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262534-G-A

224714769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262689-C-T

224714786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262705-A-G

http://identifiers.org/hco/1/GRCh38#224715022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181262912-C-A

224715022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181262912-C-T

224715166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263047-A-G

224715179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263083-C-T

224715275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263167-T-C

224715291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263179-T-C

224715350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263240-G-A

224715482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263389-G-T

224715497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181263406-C-T

http://identifiers.org/hco/1/GRCh38#224716613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181264500-A-C

224717375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181264853-G-T

224717579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265032-T-C

224717591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265044-T-C

224717687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265149-C-T

224717702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265161-G-T

224717732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265195-C-T

224717748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265211-T-A

224717748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181265211-T-C

http://identifiers.org/hco/1/GRCh38#224717798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181265245-C-A

224717864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181265322-C-T

224717920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181265375-G-T

224719470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181266560-T-G

224719480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181266632-A-G

224719583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181266735-A-G

224719644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181266778-G-C

224719953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181266935-A-G

224719976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181266958-G-A

224720061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267119-C-T

224720107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267188-A-G

224720215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267298-T-C

224720272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267348-G-T

224720322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267388-C-G

224720341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267407-G-A

224720911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181267999-A-G

224720998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181268046-G-C

224721067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181268113-C-T

224721434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181268489-G-A

224721713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181268822-A-G

224721798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181268896-G-C

224721873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181268994-C-T

224722154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269217-G-A

224722523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269491-C-G

224722572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269569-C-G

224722588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269585-T-C

224722588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269585-T-G

224722805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269800-G-A

224722863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181269861-G-T

224723049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270068-A-G

224723052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270071-G-T

224723531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270227-C-T

224723536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270232-G-T

224723744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270436-C-G

224723770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270462-G-A

224723770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270462-G-T

224723775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270467-A-G

http://identifiers.org/hco/1/GRCh38#224723793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181270485-C-A

http://identifiers.org/hco/1/GRCh38#224723794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181270486-A-C

224723893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270580-G-A

224724380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270845-A-T

224724397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181270867-A-G

224726197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181273365-G-T

224726308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181273495-G-A

224726354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181273535-G-T

224726516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181273701-T-C

224726851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181274576-T-C

224727070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181274784-C-T

224727138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181274840-G-A

http://identifiers.org/hco/1/GRCh38#224727314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181275003-A-C

224727330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275019-A-G

224727478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275191-T-C

http://identifiers.org/hco/1/GRCh38#224728038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181275678-A-C

224728147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275785-G-A

224728260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275855-G-A

224728339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275918-T-G

224728340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275919-G-T

224728425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181275998-G-T

224728477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181276044-T-C

224728833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181276398-A-G

http://identifiers.org/hco/1/GRCh38#224729811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181277074-C-A

224730151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181277338-G-T

http://identifiers.org/hco/1/GRCh38#224730238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181277371-C-A

224730238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181277371-C-T

http://identifiers.org/hco/1/GRCh38#224730426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181277498-C-A

http://identifiers.org/hco/1/GRCh38#224730454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181277527-C-A

224730476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 181277549-A-G

224730605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181277678-G-A

224730606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181277679-T-A

224730606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 181277679-T-C

224730831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181278207-C-T

224730920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181278294-T-G

224731241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181278697-T-A

224731241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181278697-T-C

224731794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181279174-T-C

224732237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181279595-C-T

224732776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181279930-G-A

224732903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181280081-A-T

224732996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181280168-T-C

224733030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181280222-C-T

224733101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181280366-G-C

224733162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181280624-A-G

224733280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181280734-G-A

224733503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181280959-A-G

224733516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181280972-G-A

224733561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181281017-C-T

224733585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181281042-A-G

224734317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181281983-T-C

224734318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181281984-G-A

224734405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282030-G-A

224734423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282047-G-A

224734423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282047-G-T

http://identifiers.org/hco/1/GRCh38#224734428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282052-A-C

224734428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282052-A-G

224734441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282065-G-A

224734441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282065-G-T

http://identifiers.org/hco/1/GRCh38#224734442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282066-C-A

224734442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282066-C-T

224734510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282104-T-C

http://identifiers.org/hco/1/GRCh38#224734513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282107-C-A

224734513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282107-C-T

http://identifiers.org/hco/1/GRCh38#224734533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282126-C-A

224734793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282389-A-G

224734800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282396-G-A

224734800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282396-G-C

224734815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282406-T-A

224734815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282406-T-G

http://identifiers.org/hco/1/GRCh38#224734821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282412-C-A

224734821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282412-C-T

224734831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282422-G-A

224734831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282422-G-T

http://identifiers.org/hco/1/GRCh38#224734836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282427-C-A

224734836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282427-C-G

224734836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282427-C-T

http://identifiers.org/hco/1/GRCh38#224734980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181282533-A-C

224735137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282690-G-A

224735414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181282948-G-C

224736483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181283324-G-C

224737158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181284379-G-A

224737158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181284379-G-T

224737343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181284515-G-T

224737445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 181284577-G-C

224737804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181284702-C-T

http://identifiers.org/hco/1/GRCh38#224737857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181284757-C-A

224738733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286297-G-A

224738901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286433-C-G

224738970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286516-G-A

224738971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286517-G-A

224739144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286641-G-A

224739147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286644-G-A

224739147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286644-G-T

224739198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286691-A-G

224739257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286735-C-G

224739257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286735-C-T

224739261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286739-A-T

224739311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 181286772-T-C

224739363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181286822-G-A

224739363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181286822-G-T

224739421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181286860-C-T

http://identifiers.org/hco/1/GRCh38#224739475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181286907-C-A

http://identifiers.org/hco/1/GRCh38#224739507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181286940-C-A

224739507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181286940-C-T

http://identifiers.org/hco/1/GRCh38#224739569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181286989-C-A

224739569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181286989-C-G

224739569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181286989-C-T

224739615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181287032-T-A

224739663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 181287077-A-G

http://identifiers.org/hco/1/GRCh38#224739772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#181287200-C-A

224739772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181287200-C-T

224739808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181287235-A-G

224739848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181287276-T-C

224739907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 181287365-G-A

224739907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 181287365-G-T

224740142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 181287614-C-G

224740413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 181287896-T-C

224740443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 181287955-T-C

http://identifiers.org/hco/1/GRCh38#224740459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#181287970-C-A

224740459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26802
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 181287970-C-T