48624515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 166408483-G-T

http://identifiers.org/hco/20/GRCh38#48624594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166408538-C-A

48624594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408538-C-T

48624642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408581-G-A

48624642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408581-G-T

48624668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408610-G-T

http://identifiers.org/hco/20/GRCh38#48624681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166408620-C-A

48624681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408620-C-T

48624863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408725-G-A

48624863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408725-G-T

48624904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408762-G-C

48624904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408762-G-T

48624925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408783-A-G

48624932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408790-G-A

48624932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408790-G-T

48624946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408803-G-C

48625029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166408881-T-C

http://identifiers.org/hco/20/GRCh38#48625260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409120-A-C

http://identifiers.org/hco/20/GRCh38#48625284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409144-C-A

48625284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409144-C-T

48625300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409160-G-A

48625300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409160-G-C

48625300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409160-G-T

http://identifiers.org/hco/20/GRCh38#48625337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409191-C-A

48625337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409191-C-T

48625411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409259-G-C

48625411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409259-G-T

48625494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409342-G-A

http://identifiers.org/hco/20/GRCh38#48625539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409381-C-A

48625539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409381-C-T

http://identifiers.org/hco/20/GRCh38#48625540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409382-C-A

48625540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409382-C-T

48625555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409406-G-T

48625738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409593-G-T

48625750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409605-G-A

48625750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409605-G-T

48625756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409612-G-A

48625756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409612-G-T

48625779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409634-G-A

48625779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409634-G-C

48625779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409634-G-T

48625807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409661-A-G

http://identifiers.org/hco/20/GRCh38#48625843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409685-C-A

48625843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409685-C-T

48625883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409726-G-A

48625883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 166409726-G-T

48625947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409791-G-A

http://identifiers.org/hco/20/GRCh38#48625966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166409808-C-A

48625966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409808-C-T

48625973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409815-G-A

48625973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409815-G-C

48625973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409815-G-T

48625975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409817-A-G

48625975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409817-A-T

48626138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166409984-G-A

48627195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410624-A-G

48627195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410624-A-T

48627209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410634-G-A

48627214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410639-G-A

48627397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410827-T-G

48627502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410927-G-A

48627502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410927-G-T

48627515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410944-G-A

48627515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410944-G-T

48627519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166410948-A-G

48627662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411085-C-G

48627662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411085-C-T

48627680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411102-G-T

48627689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411111-G-A

48627689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411111-G-T

48627694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411116-G-A

48627694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411116-G-C

48627694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411116-G-T

48627697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411118-C-T

http://identifiers.org/hco/20/GRCh38#48627711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166411132-C-A

48627846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411246-G-A

48628012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411402-T-A

48628012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411402-T-C

48628012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166411402-T-G

48629305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412104-G-A

48629305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412104-G-T

48629327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412124-A-G

48629327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412124-A-T

http://identifiers.org/hco/20/GRCh38#48629361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166412148-C-A

48629361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412148-C-T

48629416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412207-C-T

http://identifiers.org/hco/20/GRCh38#48629426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166412217-C-A

48629426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412217-C-T

48629516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 166412322-T-C

48629529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 166412335-G-A

48629549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 166412355-C-T

48629698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412483-C-T

http://identifiers.org/hco/20/GRCh38#48629701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166412486-C-A

48629701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412486-C-G

48629701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412486-C-T

http://identifiers.org/hco/20/GRCh38#48629702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166412487-A-C

http://identifiers.org/hco/20/GRCh38#48629747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166412531-C-A

48629747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412531-C-T

48629941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412681-G-A

48629958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412698-C-T

48630051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166412789-T-A

http://identifiers.org/hco/20/GRCh38#48630351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166413147-A-C

48630351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413147-A-G

48630352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413148-G-T

48630588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413360-A-G

48630589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413361-G-A

http://identifiers.org/hco/20/GRCh38#48630679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166413412-C-A

48630679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413412-C-T

48630743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 166413465-C-T

48630809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413531-T-A

48630809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413531-T-C

48630812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413534-G-A

48630812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413534-G-T

48630843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413584-C-G

48630843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413584-C-T

48630851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413592-C-G

48630851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413592-C-T

48630879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413626-C-T

48630883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413629-G-A

48630883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413629-G-T

http://identifiers.org/hco/20/GRCh38#48630885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166413631-C-A

48630885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166413631-C-T

http://identifiers.org/hco/20/GRCh38#48631330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166414007-A-C

48631822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414507-C-G

http://identifiers.org/hco/20/GRCh38#48631826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166414511-C-A

48631876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414557-C-T

48631909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414567-A-G

48631933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414591-G-C

48631993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414632-C-T

48632038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414663-C-T

48632183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414768-A-G

48632183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166414768-A-T

48632367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 166414949-G-A

48632381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 166414963-G-A

48632512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166415091-T-C

48632512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166415091-T-G

48632617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166415196-A-G

48632638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 166415217-G-A

48632638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 166415217-G-T

http://identifiers.org/hco/20/GRCh38#48632693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166415276-A-C

48632712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415299-A-G

http://identifiers.org/hco/20/GRCh38#48632754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166415356-C-A

48632754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415356-C-G

48632754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415356-C-T

48632757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415359-G-A

48632757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415359-G-T

48632806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415430-G-A

48632844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415468-C-T

48633009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415628-G-A

48633175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415786-T-C

48633200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415811-T-G

48634589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166415979-A-G

48634800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416165-G-A

48634802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416167-G-A

48634802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416167-G-T

http://identifiers.org/hco/20/GRCh38#48634813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416178-C-A

48634813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416178-C-T

48634825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416189-A-G

http://identifiers.org/hco/20/GRCh38#48634844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416206-C-A

48634844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416206-C-T

http://identifiers.org/hco/20/GRCh38#48634861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416223-C-A

48634861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416223-C-T

http://identifiers.org/hco/20/GRCh38#48634913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416262-C-A

48634922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416264-T-A

48634922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416264-T-C

48634923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416265-G-A

48635006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416347-C-T

48635113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416420-C-T

48635194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416458-T-A

48635334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416575-C-T

48635444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416687-C-T

http://identifiers.org/hco/20/GRCh38#48635551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416770-A-C

48635572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166416785-G-A

http://identifiers.org/hco/20/GRCh38#48635779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416941-C-A

http://identifiers.org/hco/20/GRCh38#48635842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#166416991-C-A

48635977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166417083-G-A

48636092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417188-C-T

48636183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417269-C-T

48636312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417361-A-G

http://identifiers.org/hco/20/GRCh38#48636352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417393-A-C

48636352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166417393-A-G

http://identifiers.org/hco/20/GRCh38#48636362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417403-C-A

48636364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417405-G-A

48636364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417405-G-C

48636364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417405-G-T

48636365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417406-G-A

48636375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417413-A-G

48636375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417413-A-T

48636376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417414-G-T

48636381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417419-T-A

48636383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417421-G-C

48636383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417421-G-T

http://identifiers.org/hco/20/GRCh38#48636457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417460-A-C

http://identifiers.org/hco/20/GRCh38#48636496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417499-C-A

48636496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417499-C-T

48636524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 166417527-T-C

http://identifiers.org/hco/20/GRCh38#48636592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417595-C-A

48636592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417595-C-T

http://identifiers.org/hco/20/GRCh38#48636601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417604-C-A

48636613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417616-G-A

48636613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417616-G-C

48636613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417616-G-T

48636619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417622-G-A

48636619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417622-G-T

48636628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417631-G-A

48636628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417631-G-T

48636640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417643-G-A

48636640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166417643-G-T

http://identifiers.org/hco/20/GRCh38#48636691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417694-C-A

48636691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 166417694-C-G

48636691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 166417694-C-T

48636695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417698-G-A

48636695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417698-G-T

48636713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417715-G-A

48636713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417715-G-T

http://identifiers.org/hco/20/GRCh38#48636729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417731-C-A

48636729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417731-C-T

48636738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417740-G-A

48636738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417740-G-T

http://identifiers.org/hco/20/GRCh38#48636753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417757-A-C

48636753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417757-A-T

48636756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417760-C-T

48636758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417762-G-A

48636758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417762-G-T

http://identifiers.org/hco/20/GRCh38#48636764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166417768-A-C

48636764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417768-A-G

48636764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417768-A-T

48636785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417786-A-G

48636813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166417799-T-A

48637035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418013-G-C

48637583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418428-T-A

48637583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418428-T-G

48637590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418435-T-C

http://identifiers.org/hco/20/GRCh38#48637621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166418463-C-A

48637621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418463-C-G

48637621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418463-C-T

http://identifiers.org/hco/20/GRCh38#48637624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166418466-C-A

48637624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418466-C-G

48637624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418466-C-T

48637692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418560-A-G

http://identifiers.org/hco/20/GRCh38#48637721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166418594-C-A

48637784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418657-G-A

48637784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418657-G-C

48637784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418657-G-T

http://identifiers.org/hco/20/GRCh38#48637792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166418665-A-C

48637792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418665-A-G

48637792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418665-A-T

48637809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418676-G-T

http://identifiers.org/hco/20/GRCh38#48637839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166418699-C-A

48637839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418699-C-T

48637848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166418702-G-A

48639623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166419700-G-T

48639634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166419711-A-G

http://identifiers.org/hco/20/GRCh38#48639635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166419712-C-A

48639635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166419712-C-T

48639990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166419997-G-A

48639990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166419997-G-T

48640003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420010-G-T

48640004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420011-A-T

48640038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420045-G-A

48640038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420045-G-C

48640038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420045-G-T

48640040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420047-G-A

48640040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420047-G-C

48640040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420047-G-T

48640048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420069-A-G

http://identifiers.org/hco/20/GRCh38#48640074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166420084-C-A

48640304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420293-G-A

http://identifiers.org/hco/20/GRCh38#48640570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166420507-C-A

48640570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420507-C-G

http://identifiers.org/hco/20/GRCh38#48640623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166420558-C-A

48640741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420734-A-G

48640751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420744-G-C

48640793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420830-G-A

48640804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420841-T-A

48640814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420851-G-A

48640866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420908-G-T

48640889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420943-G-A

48640889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420943-G-T

48640908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420972-T-C

48640908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420972-T-G

48640912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166420976-T-G

48640940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421060-G-A

48640954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421074-A-G

48640995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421114-T-C

48641056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421177-G-T

48641087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421208-G-T

48641104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421224-G-A

48641104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421224-G-T

48641109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166421229-G-C

http://identifiers.org/hco/20/GRCh38#48641960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166421983-A-C

48642017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166422039-G-A

48642017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166422039-G-C

48642017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166422039-G-T

48642051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166422071-T-A

48642051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166422071-T-C

http://identifiers.org/hco/20/GRCh38#48642055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166422075-C-A

48642055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166422075-C-T

48642303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 166422249-A-G

48642307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 166422253-A-G

http://identifiers.org/hco/20/GRCh38#48642373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166422310-C-A

48642373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 166422310-C-G

48642400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 166422330-G-T

48642492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 166422422-G-A

48642492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 166422422-G-C

48642492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 166422422-G-T

48642506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166422436-G-A

http://identifiers.org/hco/20/GRCh38#48642532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166422453-C-A

48642532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166422453-C-T

48642632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166422530-A-G

http://identifiers.org/hco/20/GRCh38#48642649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166422547-C-A

48642678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166422576-T-A

48642678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166422576-T-C

48644394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166423812-T-A

48644422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166423840-G-A

48644428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166423846-G-T

48644617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424015-G-A

48644617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424015-G-T

48644953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424233-T-G

48645015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424286-G-C

48645025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424296-C-T

48645030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424301-G-C

48645094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424368-A-G

48645467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424702-C-T

48645518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166424730-T-C

48645806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166425004-A-G

48645836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166425015-G-T

48645951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166425130-T-G

48646061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 166425246-C-T

http://identifiers.org/hco/20/GRCh38#48648703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166426469-A-C

48648711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166426477-G-T

48648810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166426602-A-T

http://identifiers.org/hco/20/GRCh38#48648946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166426709-A-C

48649064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166426790-A-T

48649128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166426829-G-A

48649148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166426849-T-C

http://identifiers.org/hco/20/GRCh38#48649197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166426897-C-A

48649197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166426897-C-T

48649243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166426919-G-T

http://identifiers.org/hco/20/GRCh38#48649260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166426936-C-A

http://identifiers.org/hco/20/GRCh38#48649373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166427025-C-A

48649373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 166427025-C-G

48649575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 166427224-G-A

48649636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427299-G-T

48649656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427322-A-G

http://identifiers.org/hco/20/GRCh38#48649853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166427509-C-A

48649853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427509-C-T

http://identifiers.org/hco/20/GRCh38#48649878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166427537-C-A

48649878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427537-C-T

48649899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427558-C-T

48649904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427563-C-T

http://identifiers.org/hco/20/GRCh38#48649920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166427578-A-C

48649920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427578-A-G

48649927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427585-G-T

48649934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427592-T-C

48649934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427592-T-G

48650015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166427672-G-A

48650015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166427672-G-T

48650036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166427693-A-G

48650081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166427738-G-A

48650087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166427744-C-T

48650181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 166427838-A-T

48650220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427883-G-T

http://identifiers.org/hco/20/GRCh38#48650231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166427894-C-A

48650231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427894-C-T

48650249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427904-G-A

48650249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427904-G-T

48650330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427979-A-G

http://identifiers.org/hco/20/GRCh38#48650351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166427997-C-A

48650351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166427997-C-T

48650663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428277-G-A

48650721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428330-C-G

48650721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428330-C-T

48650798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428392-T-A

48650897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166428446-C-T

48651026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166428575-G-A

48651089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428641-T-A

48651089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428641-T-C

48651090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428642-G-T

http://identifiers.org/hco/20/GRCh38#48651121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166428664-A-C

48651121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428664-A-G

48651129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428672-T-C

48651243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428786-G-A

48651243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428786-G-T

48651250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428793-G-T

48651276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166428819-G-T

48651432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166429003-G-A

48651492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166429063-G-A

48651513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166429084-C-G

http://identifiers.org/hco/20/GRCh38#48651516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166429087-A-C

48651549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166429120-G-A

http://identifiers.org/hco/20/GRCh38#48652573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166430861-C-A

48652573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166430861-C-T

48652576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166430864-C-T

48652677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166430950-A-G

http://identifiers.org/hco/20/GRCh38#48652711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166430984-C-A

48652873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431099-G-A

http://identifiers.org/hco/20/GRCh38#48652898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431138-C-A

48652898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431138-C-T

48653097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431303-T-A

48653097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431303-T-C

http://identifiers.org/hco/20/GRCh38#48653382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431451-C-A

48653442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166431511-A-G

48653442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 166431511-A-T

http://identifiers.org/hco/20/GRCh38#48653514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431581-C-A

48653514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431581-C-T

48653522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431589-G-A

48653522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431589-G-T

48653542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431610-A-G

http://identifiers.org/hco/20/GRCh38#48653567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431627-C-A

48653567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431627-C-G

48653567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431627-C-T

http://identifiers.org/hco/20/GRCh38#48653584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431641-A-C

48653595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431649-G-A

48653595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431649-G-T

http://identifiers.org/hco/20/GRCh38#48653632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431678-C-A

48653632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431678-C-T

http://identifiers.org/hco/20/GRCh38#48653637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431682-C-A

48653637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431682-C-T

http://identifiers.org/hco/20/GRCh38#48653643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431688-C-A

48653643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431688-C-T

48653714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431704-G-A

48653842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431778-C-T

48653891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431829-A-T

48654027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166431950-T-C

http://identifiers.org/hco/20/GRCh38#48654056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166431976-A-C

48654244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166432143-C-T

48654245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166432144-G-A

48655312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 166432376-C-T

48655380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 166432442-A-G

48655950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166432751-C-G

http://identifiers.org/hco/20/GRCh38#48656359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166433614-C-A

48656359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433614-C-T

48656361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433616-G-A

48656401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433652-G-A

48656404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433655-T-A

48656404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433655-T-C

http://identifiers.org/hco/20/GRCh38#48656489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166433694-C-A

48656489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433694-C-T

48656511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433709-C-T

48656714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433881-G-A

48656810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433972-G-A

48656828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 166433990-C-T

48656950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166434071-G-A

48656950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166434071-G-C

48656977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166434079-G-A

48656977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166434079-G-T

48657028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166434105-T-A

48657028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 166434105-T-C

48657105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 166434186-G-A

48657144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 166434225-C-T

http://identifiers.org/hco/20/GRCh38#48657171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#166434252-C-A

48657171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 166434252-C-T

48657448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 166434429-C-T

http://identifiers.org/hco/20/GRCh38#48657886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#166434583-C-A

48657886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 166434583-C-G

48657886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 166434583-C-T

48657902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 166434598-G-A

48658020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 166434659-A-G

http://identifiers.org/hco/20/GRCh38#48659263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166435029-C-A

48659263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435029-C-G

48659263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435029-C-T

48659518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435288-G-A

http://identifiers.org/hco/20/GRCh38#48659520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166435290-C-A

48659572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435363-T-C

48659572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435363-T-G

48659593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435393-C-T

48659667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435454-C-T

48659961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 166435722-G-A

48660045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, missense_variant
orthologous variants: 166435806-C-G

48660045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 166435806-C-T

http://identifiers.org/hco/20/GRCh38#48660081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166435841-C-A

48660087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435846-G-A

48660181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166435936-T-G

48662223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166436801-C-T

48662681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166437165-A-T

48662742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166437219-G-C

48662757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166437234-T-C

48666299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: start_lost, synonymous_variant
orthologous variants: 166438222-A-G

48666414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166438327-G-A

48666414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166438327-G-T

48666422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166438335-G-T

48667955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166439145-C-T

48676273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 166441606-G-A

48676301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166441635-C-G

48679044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443167-T-G

48679104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443215-C-T

48679113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443224-G-A

48679124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443235-G-A

48679166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443276-T-C

48679166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443276-T-G

48679268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443365-G-A

48679268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443365-G-T

48679322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443404-G-A

48679322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443404-G-C

48679322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443404-G-T

48679326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443408-G-A

48679340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443422-G-T

48679480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166443544-G-T

48679775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166443768-G-A

48679775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166443768-G-T

48679790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166443783-C-T

48679854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166443793-G-A

48679854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166443793-G-T

http://identifiers.org/hco/20/GRCh38#48680150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166443950-A-C

48680413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444096-T-C

48680515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444128-G-C

48680720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444292-G-A

48680720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444292-G-C

48680803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444375-T-C

48680874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444427-A-G

48680916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444470-C-T

48681074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444599-G-A

48681097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444621-C-T

http://identifiers.org/hco/20/GRCh38#48681116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166444635-C-A

48681116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444635-C-T

48681142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444661-G-T

48681147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444666-G-A

48681147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444666-G-C

48681149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444668-G-C

48681149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444668-G-T

48681155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444674-T-C

48681208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444711-C-T

48681212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444715-G-A

48681212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444715-G-C

48681212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444715-G-T

48681251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: missense variant
orthologous variants: 166444752-A-T

48681376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444876-T-C

48681474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444965-T-C

48681474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166444965-T-G

48681615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166445098-G-A

48681662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166445144-G-T

http://identifiers.org/hco/20/GRCh38#48681729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166445201-C-A

48681729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166445201-C-G

48681811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166445301-G-A

48682700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447121-G-A

48682710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447133-G-A

48682710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447133-G-C

http://identifiers.org/hco/20/GRCh38#48682763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166447183-A-C

48682917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447294-G-C

48682974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447348-C-T

48682975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447349-G-A

48682984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447356-T-C

48682988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447360-G-T

48683004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447376-G-C

48683331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166447680-G-A

48683741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448069-A-G

48683814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448106-T-G

48683923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448178-G-C

48683965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448214-T-C

48683965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448214-T-G

http://identifiers.org/hco/20/GRCh38#48684129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166448350-C-A

48684129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448350-C-T

http://identifiers.org/hco/20/GRCh38#48684237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166448440-C-A

48684542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448728-A-G

http://identifiers.org/hco/20/GRCh38#48684747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166448860-A-C

48684803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448900-G-A

48684832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448923-C-T

48684855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166448942-A-G

48685211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166449343-G-A

http://identifiers.org/hco/20/GRCh38#48685298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166449451-C-A

48685298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166449451-C-T

48685338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166449508-G-C

48685454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166449639-C-T

48686233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166450352-C-T

48686273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166450386-G-A

48686335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166450437-C-T

48686651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166450724-C-G

48686651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166450724-C-T

48686730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166450810-G-A

48688415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451428-T-C

48688453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451460-G-C

http://identifiers.org/hco/20/GRCh38#48688516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166451517-C-A

48688516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451517-C-T

48688529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451530-G-C

48688529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451530-G-T

48688554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451572-T-C

48688593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451620-A-T

http://identifiers.org/hco/20/GRCh38#48688607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166451624-C-A

http://identifiers.org/hco/20/GRCh38#48688629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166451643-C-A

48688752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166451753-C-T

48688791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 166451792-G-C

http://identifiers.org/hco/20/GRCh38#48688877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166451844-C-A

48688877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451844-C-T

http://identifiers.org/hco/20/GRCh38#48688891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166451849-C-A

48688901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451859-G-A

48688901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451859-G-C

48688901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451859-G-T

48688976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166451924-C-T

48689077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452005-C-T

48689401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452200-A-G

48689448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452233-G-A

48689574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452392-T-A

48689617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452453-A-G

48689671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452510-A-G

48689686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452524-C-G

48689876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452677-A-G

48689876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452677-A-T

48689920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452712-C-T

48689938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452727-A-G

48689989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452777-A-G

48690241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166452962-G-A

http://identifiers.org/hco/20/GRCh38#48690486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166453141-A-C

48690689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453318-C-T

48690787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453391-G-A

48690790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453394-T-C

http://identifiers.org/hco/20/GRCh38#48690865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166453486-C-A

48690865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453486-C-G

48690923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453532-G-A

48690923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453532-G-T

48690929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453534-C-T

48690940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 166453541-T-G

48691020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 166453621-G-C

48691059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166453660-G-A

48691071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166453672-G-A

48691071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166453672-G-C

http://identifiers.org/hco/20/GRCh38#48691137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166453741-C-A

48691137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453741-C-T

48691139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453743-C-T

48691145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453749-C-T

48691157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453761-C-T

http://identifiers.org/hco/20/GRCh38#48691199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166453779-C-A

48691264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166453861-G-A

48691581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166454038-C-T

48692155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166454533-G-A

48692356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454808-T-C

48692356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454808-T-G

48692385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454832-T-C

48692407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454872-G-A

48692407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454872-G-T

48692408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454873-A-G

48692408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454873-A-T

48692424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454882-G-C

48692424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454882-G-T

48692445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454903-G-A

48692445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454903-G-T

48692559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454971-G-A

48692559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166454971-G-C

http://identifiers.org/hco/20/GRCh38#48692590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166455002-A-C

48692590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166455002-A-G

48692590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166455002-A-T

48692591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166455003-T-A

48692591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166455003-T-C

http://identifiers.org/hco/20/GRCh38#48692645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166455037-C-A

48692645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 166455037-C-T

http://identifiers.org/hco/20/GRCh38#48692679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166455069-A-C

48692744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: missense variant
orthologous variants: 166455134-C-T

48692889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455241-G-A

48692889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455241-G-T

48692908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455260-A-G

48692929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455282-G-A

48692929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455282-G-T

48693139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455503-C-T

48693217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166455576-T-C

48694221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166456276-G-A

48694256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166456311-T-A

48697829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457246-C-G

48698044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457437-C-G

48698246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457632-T-A

48698324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457707-T-C

48698520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457893-G-A

48698566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457915-G-A

48698566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457915-G-T

48698651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166457984-G-A

48698793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458102-C-T

48698875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458177-G-A

48699080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458334-G-A

48699154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458384-C-G

48699517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458679-C-T

48699605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458769-G-A

http://identifiers.org/hco/20/GRCh38#48699725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166458893-C-A

48699738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166458903-A-G

http://identifiers.org/hco/20/GRCh38#48699857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166459040-A-C

48700120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166459306-G-A

48700180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166459360-A-G

48700367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166459517-G-A

http://identifiers.org/hco/20/GRCh38#48700691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166459665-C-A

48700821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166459821-C-T

48700909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166459908-G-A

48700927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166459923-G-T

48707190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166461747-G-C

48707192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166461749-G-A

48707192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166461749-G-C

48707282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166461831-G-A

48707310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166461845-G-A

48707588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166462074-C-T

48707964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166462832-A-G

48708019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166462890-G-A

48708058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166462924-T-C

48708058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166462924-T-G

http://identifiers.org/hco/20/GRCh38#48708153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166463004-C-A

48708184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166463030-G-T

http://identifiers.org/hco/20/GRCh38#48708186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166463032-C-A

48708186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166463032-C-T

http://identifiers.org/hco/20/GRCh38#48708201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166463047-C-A

48708201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166463047-C-T

48708380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166463212-G-A

48708380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: synonymous variant
orthologous variants: 166463212-G-C

48708441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166463270-G-A

48708441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166463270-G-C

48708461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166463282-C-T

48712536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166465162-T-C

48712768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166465374-T-C

48715014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166466676-A-G

48715293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166466939-T-A

48715293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166466939-T-C

48715380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467027-T-A

48715380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467027-T-G

48715409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467055-C-T

48715410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467056-C-G

48715638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467210-T-C

48715655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467227-C-T

48715668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467240-A-G

48715680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467252-C-T

48715687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467259-A-G

48715712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467285-T-C

48716158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467580-G-A

48716228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467635-A-G

48716265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467670-G-A

48716355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467757-A-T

48716366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467768-G-A

48716397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166467800-T-C

http://identifiers.org/hco/20/GRCh38#48716449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166467860-C-A

48716679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166468041-G-A

48717166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166468521-C-T

48717341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166468700-T-C

48717395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166468755-C-T

48717485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166468838-C-T

48722855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166471750-T-C

48723208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472126-G-A

48723344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472249-T-G

48723408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472306-C-T

48723431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472328-G-A

48723489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472383-A-G

48723512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472405-A-G

48723610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472459-G-A

48723887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166472689-C-T

48724006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472819-T-G

48724024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472835-A-G

48724068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472873-A-G

48724082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472887-G-A

48724131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166472939-A-G

48724269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166473058-C-T

48724302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166473065-G-A

48724371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166473128-T-C

48724565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166473370-C-T

48724582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166473378-T-C

48724742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166473552-C-G

48725048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166474096-T-C

48725371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166474417-G-A

48725526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166474560-T-C

48725722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166474705-A-T

48725874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166474864-G-C

48726134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475126-G-T

http://identifiers.org/hco/20/GRCh38#48726178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166475163-C-A

48726178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475163-C-T

http://identifiers.org/hco/20/GRCh38#48726184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166475169-C-A

48726409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475406-A-T

48726457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475439-A-G

http://identifiers.org/hco/20/GRCh38#48726541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166475506-A-C

48726541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475506-A-G

48726541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475506-A-T

48726667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475622-T-C

48726844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475866-C-T

48726853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475875-G-A

48726853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166475875-G-C

http://identifiers.org/hco/20/GRCh38#48728332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166477402-A-C

48728373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477441-C-T

48728388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477455-G-C

48728450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477520-T-C

48728540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477604-G-A

48728540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477604-G-C

48728555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477619-C-T

48728556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477620-G-A

48728570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166477634-G-A

48732081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479252-G-A

48732243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479395-C-T

48732381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479561-T-C

48732433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479613-T-C

48732616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479789-T-C

48732616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479789-T-G

48732705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166479864-G-C

48734527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480222-G-C

48734624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 166480313-C-T

48734630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 166480319-G-A

48734741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480399-G-A

48734741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480399-G-C

48734741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480399-G-T

http://identifiers.org/hco/20/GRCh38#48734753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166480411-C-A

48734753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480411-C-T

48734778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166480438-G-T

http://identifiers.org/hco/20/GRCh38#48734788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166480447-A-C

48734788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480447-A-G

48735041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166480683-A-G

48738593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166482847-G-A

48738623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166482877-G-A

48738740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166482998-G-A

48738868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166483092-A-G

48738911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166483122-G-A

48739173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166483340-T-C

48739262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166483427-C-T

48741991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166486332-G-C

48742138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166486419-G-A

48745120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 166486764-G-C

48745175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166486812-A-G

48745197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166486833-G-A

48745197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166486833-G-C

48746369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166487512-T-C

48746378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166487521-C-T

48746402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166487545-T-C

48746799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488047-C-T

48746801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488049-T-A

48746801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488049-T-C

http://identifiers.org/hco/20/GRCh38#48747031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166488225-A-C

48747211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488380-G-C

48747624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488720-G-A

48747698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488789-G-A

48747698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488789-G-T

http://identifiers.org/hco/20/GRCh38#48747699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166488790-C-A

48747699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488790-C-G

48747699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488790-C-T

48747704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488795-G-A

48747704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488795-G-T

48747725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488805-A-G

http://identifiers.org/hco/20/GRCh38#48747800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166488885-C-A

48747800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488885-C-G

48747800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166488885-C-T

48747848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 166488933-G-A

48747958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489039-G-A

48747958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489039-G-T

48747960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489041-T-C

48747962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489042-A-G

48747992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489070-G-A

48747992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489070-G-T

48748136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166489209-C-T

http://identifiers.org/hco/20/GRCh38#48749282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166490027-C-A

48749282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166490027-C-T

48749373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166490088-G-A

48750285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491122-C-G

48750309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491146-A-G

48750335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491184-G-A

48750433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491283-C-T

48750584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491387-C-T

48750596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491398-G-A

48750596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491398-G-T

48750743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491513-G-A

48750760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491530-A-G

48750894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166491661-G-A

48751049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492238-C-T

48751058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492247-G-A

48751072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492261-C-T

48751352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166492515-C-T

48751507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492674-G-A

48751580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492744-C-G

48751642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492797-C-G

48751788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166492925-T-G

48752065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166493168-C-T

48754404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166495548-C-G

48754404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166495548-C-T

48754539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166495665-C-T

48754583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166495709-T-C

48754913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166495985-G-A

48754941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166496013-T-A

48755085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166496156-A-T

http://identifiers.org/hco/20/GRCh38#48755121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166496191-C-A

48755121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166496191-C-G

http://identifiers.org/hco/20/GRCh38#48761119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166497881-A-C

48761184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166497933-G-C

48761197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166497946-G-A

48761244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166497982-C-T

http://identifiers.org/hco/20/GRCh38#48761263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166498011-A-C

48761282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498030-A-G

48761307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498057-T-C

48761351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498058-T-A

48761457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498144-T-C

48761466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498153-C-T

48762113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498644-G-A

48762399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166498948-C-T

48762595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499080-T-C

48762861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499212-C-T

48763020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499253-T-G

48763040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499268-A-T

48763120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499327-G-C

48763178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499372-G-C

48763293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499437-G-A

48763342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499485-T-A

48763399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499540-A-G

48763410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499552-C-T

48763414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499556-G-A

48763431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499573-G-A

48763431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499573-G-T

48763436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499578-G-T

48763509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499642-G-A

48763652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499783-T-C

48763855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499953-G-A

48763871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499959-G-A

48763871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499959-G-C

48763874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499962-G-A

48763874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499962-G-T

48763882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166499976-T-C

48763917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500010-A-G

48764002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500080-A-T

48764016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500094-T-G

48764031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500110-C-G

48764080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500143-C-T

48764081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500144-G-A

48764164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500224-G-T

48764229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166500263-G-A

48769588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166502520-T-A

48769616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166502551-C-T

48776020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505008-G-A

48776049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505035-A-G

48776245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505231-A-G

48776292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505275-T-C

48776292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505275-T-G

http://identifiers.org/hco/20/GRCh38#48776593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166505561-C-A

48776593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505561-C-T

48776685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505633-G-T

48776746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166505698-C-T

48785234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511415-T-C

48785253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511436-G-A

48785255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511442-G-A

48785343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511534-C-T

48785354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511546-G-A

48785354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511546-G-T

48785547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511682-G-A

48785601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511715-G-A

48785610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511723-C-T

48785673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166511788-G-T

48786093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512327-C-G

48786209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512451-G-C

http://identifiers.org/hco/20/GRCh38#48786387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166512588-C-A

48786439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512639-T-A

48786439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512639-T-G

48786512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512666-G-A

48786825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512803-G-A

48786825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512803-G-C

48786825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512803-G-T

http://identifiers.org/hco/20/GRCh38#48786974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166512944-C-A

48786974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512944-C-T

48787006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166512973-C-T

48787072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166513021-G-A

48787103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166513052-G-A

http://identifiers.org/hco/20/GRCh38#48787154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166513101-C-A

48787196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166513121-G-A

48787260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166513188-C-G

48787260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166513188-C-T

48787277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166513216-G-A

http://identifiers.org/hco/20/GRCh38#48788003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166514464-C-A

48788182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166514632-A-G

48788238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166514666-T-C

48788515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166514873-G-A

48790311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166517817-A-G

http://identifiers.org/hco/20/GRCh38#48790395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166517936-A-C

48790395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166517936-A-G

48790453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166517989-G-A

48790506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518045-G-A

48790677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518193-G-C

48790708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518225-A-G

48790708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518225-A-T

http://identifiers.org/hco/20/GRCh38#48790744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166518259-C-A

48790744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518259-C-T

48790750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518265-A-G

48791041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518484-G-A

48791155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166518561-A-G

http://identifiers.org/hco/20/GRCh38#48791472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166518794-A-C

48791472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518794-A-G

48791603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518880-G-A

48791617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166518889-G-A

48793924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166520437-C-G

48793971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166520484-T-C

http://identifiers.org/hco/20/GRCh38#48793986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166520507-C-A

48794034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166520566-C-T

http://identifiers.org/hco/20/GRCh38#48794129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166520640-C-A

48794286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166520813-C-G

48794492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166520975-T-C

48795056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522204-T-A

48795374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522558-C-T

http://identifiers.org/hco/20/GRCh38#48795430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166522599-A-C

http://identifiers.org/hco/20/GRCh38#48795433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166522602-A-C

48795808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522846-C-G

48795830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522867-C-T

48795914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522931-G-A

48795919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522936-C-G

48795919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522936-C-T

48795966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522960-A-G

48796002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166522998-G-A

48796005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166523001-G-A

48796005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166523001-G-C

48796999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166524578-G-T

48797143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166524730-T-C

48797326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166524888-G-A

48797326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166524888-G-T

48797532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166525070-C-T

48797640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166525173-G-A

48797650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166525183-G-A

48797650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166525183-G-C

48797884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166525354-G-C

48799590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166526495-A-G

48799629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166526518-C-G

48799829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166526619-G-A

48799917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166526695-G-A

http://identifiers.org/hco/20/GRCh38#48800162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166526912-C-A

48800162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166526912-C-T

48803222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166527783-T-C

48803350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166527898-G-A

48803526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528039-G-A

48803581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528108-C-T

48803775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528276-G-A

48803775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528276-G-C

48803866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528356-C-T

48804014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528486-A-G

48804269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528632-A-G

48804276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528639-A-G

48804556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528867-G-A

48804583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528876-G-A

48804585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166528878-G-A

48804754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529073-G-T

48804760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529079-A-G

48804813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529131-G-A

http://identifiers.org/hco/20/GRCh38#48804876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166529177-A-C

48804876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529177-A-T

48805165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529434-G-A

48805532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529712-T-C

48805601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166529762-C-T

48807890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166534058-G-A

48807981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166534145-G-A

48808212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166534360-G-A

48808212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166534360-G-T

48808282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166534428-A-G

48809676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166535431-C-T

48809697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166535445-G-T

48809776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166535481-C-G

http://identifiers.org/hco/20/GRCh38#48814107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166539998-C-A

48814121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166540037-T-C

48814269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166540267-A-G

48814775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166540684-G-A

48815129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166541005-G-C

http://identifiers.org/hco/20/GRCh38#48815688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166541511-C-A

48817234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166542391-A-G

48817482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166542563-C-T

48818049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166543128-T-C

48818149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, undefined
orthologous variants: 166543226-G-A

48818538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166543469-C-T

48818551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166543482-T-C

48818693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166543590-C-T

48818707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166543613-A-G

48818851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166543802-G-A

48819083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166544010-C-T

48819207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166544142-C-G

http://identifiers.org/hco/20/GRCh38#48819369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166544290-A-C

48819588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166544500-T-A

48819740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166544709-G-A

48819740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166544709-G-C

48819809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166544828-C-G

48819987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166544955-A-G

48820074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545016-T-C

48820110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545055-G-A

48820243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545172-C-T

http://identifiers.org/hco/20/GRCh38#48820418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166545369-C-A

48820418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545369-C-G

48820814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545747-C-T

48821285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545825-T-C

48821370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166545890-C-T

48821492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166546008-A-G

48821601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166546099-G-A

48821601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166546099-G-T

48821617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 166546109-A-G

48821677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron variant
orthologous variants: 166546155-T-C

48821734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166546176-G-C

48821734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 166546176-G-T

48822979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166551915-A-G

48823171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166552103-C-T

http://identifiers.org/hco/20/GRCh38#48824062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166552717-C-A

48824062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166552717-C-T

48824117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166552752-G-A

48824117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166552752-G-T

48824128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166552763-C-T

48824230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 166552859-A-G

48824265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 166552907-G-C

http://identifiers.org/hco/20/GRCh38#48824407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166553047-C-A

48824464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 166553099-T-C

http://identifiers.org/hco/20/GRCh38#48824778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166553413-A-C

48825098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166553733-T-C

48825182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166553815-G-A

48825182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166553815-G-C

48825185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166553818-G-A

48825251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 166553878-G-A

48825536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554148-C-T

48825575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554184-C-G

48825706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554287-T-C

48825829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554407-G-A

http://identifiers.org/hco/20/GRCh38#48825860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166554486-A-C

48825860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554486-A-T

48825888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554510-G-A

48825888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554510-G-C

48826054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166554633-T-C

http://identifiers.org/hco/20/GRCh38#48826167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166554731-A-C

48826557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166555099-A-G

48827820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 166555598-G-A

48827820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 166555598-G-C

48827820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 166555598-G-T

48827828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 166555606-G-A

48827828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 166555606-G-C

48827828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 166555606-G-T

48827842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 166555620-T-C

48827943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 166555713-C-G

48827943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 166555713-C-T

http://identifiers.org/hco/20/GRCh38#48827972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166555735-C-A

48827972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 166555735-C-T

48828004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166555767-G-A

48828004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166555767-G-C

48828004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166555767-G-T

http://identifiers.org/hco/20/GRCh38#48828010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#166555773-C-A

48828010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166555773-C-T

48828013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166555776-C-T

48828339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 166556071-A-T

48829016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166556606-G-T

48829307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166556835-G-A

48829645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166557144-C-T

48830023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166557420-C-T

48830225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 166557522-G-C