http://identifiers.org/hco/12/GRCh38#101877595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88192965-C-A

101877595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192965-C-G

101877595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192965-C-T

101877640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192922-T-C

101877654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192908-T-A

101877654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192908-T-C

http://identifiers.org/hco/12/GRCh38#101877666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88192896-C-A

101877666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192896-C-G

101877666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192896-C-T

101877671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192891-A-G

http://identifiers.org/hco/12/GRCh38#101877682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88192881-C-A

101877682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 5 prime UTR variant
orthologous variants: 88192881-C-T

http://identifiers.org/hco/12/GRCh38#101877892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88192680-C-A

101877892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192680-C-G

101877892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192680-C-T

101877998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192596-G-A

101877998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192596-G-T

http://identifiers.org/hco/12/GRCh38#101878012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88192582-C-A

101878054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192541-G-T

101878129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192476-C-T

101878136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192469-C-G

101878136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192469-C-T

101878242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192350-T-C

101878254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192339-A-T

101880641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88190889-G-C

101880690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88190839-G-A

101880812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88190721-G-T

101880908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88190619-T-G

101880969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88190570-G-T

101884085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88186956-A-G

101891812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88184989-T-C

101892188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88184379-T-A

101892275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88184318-G-A

101892275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88184318-G-T

101892395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88184203-C-G

101894872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88182520-G-A

101894922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88182483-G-A

101895023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88182383-G-C

http://identifiers.org/hco/12/GRCh38#101896450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88181907-A-C

101897161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88181522-G-A

http://identifiers.org/hco/12/GRCh38#101897732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88180701-C-A

101897732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88180701-C-T

101897787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88180649-T-C

101897811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88180629-G-A

101898823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88178247-C-G

101898849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88178215-G-C

101898904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88178159-A-G

101898946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88178116-A-G

101901092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176751-T-C

http://identifiers.org/hco/12/GRCh38#101901130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88176713-C-A

101901130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176713-C-T

101901174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176663-G-T

101901208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176595-A-T

101901219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176584-C-G

http://identifiers.org/hco/12/GRCh38#101901224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88176579-C-A

http://identifiers.org/hco/12/GRCh38#101901268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88176547-A-C

101901272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176543-A-G

101901279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88176534-C-T

101901382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88176431-A-G

101901471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88176342-G-T

http://identifiers.org/hco/12/GRCh38#101901496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88176317-C-A

101901520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88176293-G-T

101902845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88175481-A-G

101902878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88175450-T-C

101903294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88175334-G-A

101903320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88175304-C-G

http://identifiers.org/hco/12/GRCh38#101908107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88172934-C-A

101908107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88172934-C-T

http://identifiers.org/hco/12/GRCh38#101908111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88172930-C-A

101908219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88172815-G-A

101908288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88172746-C-G

101908288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88172746-C-T

101908456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88172560-G-A

101908551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88172487-A-G

101908564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88172474-G-A

101909492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88171093-T-C

http://identifiers.org/hco/12/GRCh38#101909520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88171065-C-A

101909520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88171065-C-T

101909540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88171053-C-T

101909760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88170844-A-G

101910328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88169520-A-G

http://identifiers.org/hco/12/GRCh38#101912426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88166885-A-C

101912533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88166797-G-A

http://identifiers.org/hco/12/GRCh38#101912569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88166765-A-C

101912636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88166696-G-A

101912680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88166653-A-G

101912688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88166645-G-A

101913276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88166198-A-G

101913746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88165822-T-A

101914129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88165043-G-C

101914129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88165043-G-T

101914145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88165036-T-C

101914297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88164883-G-A

101914297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88164883-G-T

101918430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88162625-A-G

101918454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88162601-T-A

101919595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161796-A-G

101919708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161683-C-T

101919757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161626-C-T

101919765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161618-A-G

http://identifiers.org/hco/12/GRCh38#101919872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88161521-C-A

http://identifiers.org/hco/12/GRCh38#101919903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88161493-A-C

http://identifiers.org/hco/12/GRCh38#101919975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88161419-C-A

101919975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161419-C-T

101919979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161415-T-C

101919995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88161399-A-G

101920245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161147-G-T

http://identifiers.org/hco/12/GRCh38#101920412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88161085-A-C

101920412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161085-A-G

101920432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161072-T-C

101920432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161072-T-G

101920469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161038-A-G

101920477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88161030-C-T

101920818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160854-G-A

101921131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160727-T-C

101921146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160712-G-A

101921146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160712-G-T

http://identifiers.org/hco/12/GRCh38#101921188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88160673-A-C

101921194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88160667-T-C

101921265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160596-A-G

101921293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160568-T-C

http://identifiers.org/hco/12/GRCh38#101921362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88160503-C-A

101921362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160503-C-T

http://identifiers.org/hco/12/GRCh38#101921432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88160432-C-A

101921432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160432-C-T

101921440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160424-A-G

101921524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160343-A-G

101921534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160333-T-C

101921538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88160329-A-G

101921783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88160084-C-G

http://identifiers.org/hco/12/GRCh38#101921907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88159957-C-A

101922095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159794-G-T

101922209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159699-T-C

http://identifiers.org/hco/12/GRCh38#101922300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88159629-C-A

http://identifiers.org/hco/12/GRCh38#101922427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88159565-A-C

http://identifiers.org/hco/12/GRCh38#101922450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88159542-C-A

101922450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159542-C-T

101922458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159535-G-A

http://identifiers.org/hco/12/GRCh38#101922530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88159461-C-A

101922530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159461-C-T

101923250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159262-T-C

101923278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159235-G-T

101923312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159202-G-C

101923312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159202-G-T

101923355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88159158-T-C

101923523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88159036-G-A

101923558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88159007-G-T

101923563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88159002-G-A

101923899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88158699-G-T

http://identifiers.org/hco/12/GRCh38#101923900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88158698-C-A

101923900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88158698-C-T

101924305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158311-G-C

101924305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158311-G-T

101924332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88158238-T-C

http://identifiers.org/hco/12/GRCh38#101924659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88157986-C-A

101924659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88157986-C-G

101924711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88157941-A-G

101925044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88157674-C-T

101925206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88157415-C-T

101925235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88157387-C-T

101925496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88157106-G-T

101926153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88156775-G-A

101926206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88156724-G-A

101926207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88156723-G-A

101929290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88153821-G-T

101931747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88151315-G-A

101931776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88151284-C-T

http://identifiers.org/hco/12/GRCh38#101931777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88151283-A-C

101931841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88151221-A-G

101931868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88151194-G-A

101931944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88151121-C-T

101932000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88151067-C-T

101932201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88150863-G-T

101932491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88150547-T-C

101932629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88150408-T-C

101932864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88150173-G-A

101932909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88150129-C-T

101933163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88149994-C-T

101933246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88149912-G-A

http://identifiers.org/hco/12/GRCh38#101933276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88149882-A-C

101933304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88149801-T-C

101933445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88149615-T-C

101933757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88149284-C-T

101933773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88149272-G-T

101934334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88148815-A-G

101934334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88148815-A-T

101934908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88147805-A-T

http://identifiers.org/hco/12/GRCh38#101935018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88147691-A-C

101935223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88147499-T-C

http://identifiers.org/hco/12/GRCh38#101935374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88147392-C-A

101935374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88147392-C-T

101935681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88147096-G-T

101935961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88146340-G-A

101935961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88146340-G-T

101935966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88146335-G-A

101936113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88146197-G-A

101936113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88146197-G-T

101936114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88146196-A-G

http://identifiers.org/hco/12/GRCh38#101936207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#88146101-C-A

101936231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 88146077-C-T

101936327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88145998-A-T

101936328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88145997-G-T

101936791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88145539-T-C

101936894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88145451-A-G

101937011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88145348-G-A

101937235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88144850-T-A

101937243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88144842-G-A

101937519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88144568-A-G

101937707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88144333-G-A

101938305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88143764-T-C

101938357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88143715-T-C

101938407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88143674-A-T

101938982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88141219-A-G

http://identifiers.org/hco/12/GRCh38#101939003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88141202-C-A

101939157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88141074-G-A

101939241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88140991-A-G

http://identifiers.org/hco/12/GRCh38#101939271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88140961-C-A

101939406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88140795-C-T

101939738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88140576-C-T

101939800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88140513-A-G

101940126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88140182-A-G

101940275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88140034-T-C

101940403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88139852-T-C

101940408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88139847-T-G

101940993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88139397-C-T

101941183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88139216-C-G

101942114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88138377-C-T

101945432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88133281-G-C

101945434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88133279-G-A

101945483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88133235-C-T

101945763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132963-G-T

101945857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132905-A-G

101945876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132886-C-T

101946031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132545-T-C

101946155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132427-T-C

101946277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132295-G-A

101946277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132295-G-C

101946448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132147-T-C

101946493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88132109-T-A

101946925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88131633-C-T

101946993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88131541-G-A

101947025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88131514-T-C

101947367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88131235-C-T

101948128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88130735-T-C

101948209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88130650-T-C

http://identifiers.org/hco/12/GRCh38#101954629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88126442-C-A

101954629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88126442-C-G

101954792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88126299-C-T

101954856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88126273-T-C

101954892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88126237-A-G

http://identifiers.org/hco/12/GRCh38#101954901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88126228-C-A

101954901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88126228-C-G

101954901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88126228-C-T

101955047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88126095-A-G

101955089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125358-A-G

101955246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125228-A-G

101955300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125176-A-G

101955371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125145-T-C

http://identifiers.org/hco/12/GRCh38#101955376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88125140-C-A

101955477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125050-C-T

101955480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125047-T-A

101955480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88125047-T-C

101955543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124986-G-T

101955561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124969-G-A

101955561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124969-G-T

101955563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124967-T-C

101955563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124967-T-G

101955579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124951-A-G

101955587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124943-A-G

101955626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124904-C-T

101955655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124876-A-G

101955656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124875-A-G

101955656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124875-A-T

101955661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124870-A-G

http://identifiers.org/hco/12/GRCh38#101955777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88124776-C-A

101955799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88124754-A-G

101955976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124630-A-G

101956650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124531-A-G

101956714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124476-C-T

101956824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124362-T-C

101956888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124291-G-A

101956977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124202-G-A

101957064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88124129-G-A

http://identifiers.org/hco/12/GRCh38#101957105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88124089-C-A

http://identifiers.org/hco/12/GRCh38#101957300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88123896-A-C

http://identifiers.org/hco/12/GRCh38#101957361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88123834-C-A

101957381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88123814-G-T

101957399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88123796-A-G

http://identifiers.org/hco/12/GRCh38#101957453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88123677-A-C

101957453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88123677-A-G

101957453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88123677-A-T

101957518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88123582-T-C

101957639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88123467-G-A

101958009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88123087-T-G

http://identifiers.org/hco/12/GRCh38#101958134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88122944-C-A

101958182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88122873-T-C

101958377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88122679-C-G

101958377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88122679-C-T

101958663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88122425-A-G

101958714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88122380-G-C

101960677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88121235-G-A

http://identifiers.org/hco/12/GRCh38#101960705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88121197-A-C

101960705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88121197-A-G

101961357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88120870-A-T

101961391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88120837-A-T

101961412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88120822-C-T

101961564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88120670-T-G

http://identifiers.org/hco/12/GRCh38#101963192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88117827-C-A

101963192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88117827-C-T

101963664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88117349-A-G

101963683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88117330-T-G

http://identifiers.org/hco/12/GRCh38#101965866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88117057-C-A

http://identifiers.org/hco/12/GRCh38#101965975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88116958-A-C

101965975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88116958-A-G

101966084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88116851-T-C

http://identifiers.org/hco/12/GRCh38#101966122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88116811-C-A

101966763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88113677-A-G

101967102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88113433-G-A

101967153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88113382-G-A

101967499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88113097-G-A

101967499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88113097-G-T

101968101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88112918-T-A

101968148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88112876-G-A

101968195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88112843-C-T

101968779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88112183-T-C

101968782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88112180-A-G

101973600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109985-G-A

101973732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109878-A-G

101973957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109638-C-T

101974000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109599-G-A

101974084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109518-T-A

101974185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109412-G-C

101974319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109291-C-T

101974330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88109280-A-G

101974780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88104737-C-T

101975516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88102463-T-C

101975731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88102243-T-C

101975766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88102207-T-C

101975877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88102089-T-G

101976001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101978-C-T

101976060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101926-T-A

101976076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101910-A-T

101976135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101853-A-G

http://identifiers.org/hco/12/GRCh38#101976319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88101671-A-C

101976319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101671-A-G

101976735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101298-A-G

101976847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88101185-C-T

101977155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100898-T-C

101977267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100790-C-G

101977385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100672-C-T

101977491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100563-A-G

101977537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100529-T-C

101977557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100509-G-T

101977589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100467-T-C

101977715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100319-C-T

101977835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100193-A-G

101977876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88100152-G-A

101978093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099939-G-T

101978112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099920-A-G

101978139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099894-A-G

101978208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099854-G-A

101978257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099815-T-C

101978332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099757-A-G

101978628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88099465-T-A

101980076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098844-T-C

101980467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098490-T-C

101980548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098411-A-G

101980563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098393-T-C

101980563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098393-T-G

101980642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098315-G-A

101980792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098170-C-G

101980924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88098030-A-G

101981243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88097615-C-T

101981387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88097459-C-G

101981826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88097019-A-G

101982078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096751-C-T

101982084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096745-G-C

101982110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096719-A-G

101982216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096569-T-C

101982241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096544-C-T

101982358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096431-C-G

101982358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096431-C-T

101982359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096430-G-A

101982359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096430-G-T

101982450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096343-C-T

101982572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096203-T-G

101982718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88096052-G-A

101983343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88087911-C-T

101983394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88087860-G-A

http://identifiers.org/hco/12/GRCh38#101983458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88087801-A-C

101983679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88087389-T-C

101983920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88087159-T-C

101984050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88087069-T-C

101984269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88086877-T-C

http://identifiers.org/hco/12/GRCh38#101984624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88086422-C-A

101984624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88086422-C-T

101984987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88086137-C-G

101984996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88086130-T-C

101985079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88086056-T-C

102011788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25645
most severe consequence: intron variant
orthologous variants: 88082397-C-G