http://identifiers.org/hco/2/GRCh38#95851657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118494817-C-A

95851719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118494882-T-C

95851719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118494882-T-G

http://identifiers.org/hco/2/GRCh38#95851763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118494926-C-A

95851763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118494926-C-G

95851763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118494926-C-T

95851808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: 118494970-T-C

95851824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: 118494987-T-A

95851824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: 118494987-T-C

http://identifiers.org/hco/2/GRCh38#95851876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118495038-C-A

95851876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: 118495038-C-T

95852042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: 118495226-T-C

95852068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron variant
orthologous variants: 118495252-C-T

95852158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118495334-T-A

95852158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118495334-T-G

95852183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense variant
orthologous variants: 118495359-T-A

95852348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495426-T-C

95852354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495432-T-A

95852354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495432-T-C

http://identifiers.org/hco/2/GRCh38#95852387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118495464-C-A

95852387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495464-C-T

95852426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495497-G-A

http://identifiers.org/hco/2/GRCh38#95852427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118495498-C-A

95852427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495498-C-T

http://identifiers.org/hco/2/GRCh38#95852436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118495507-C-A

95852436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495507-C-T

95852445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495520-G-A

95852445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495520-G-T

95852494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118495565-C-T

http://identifiers.org/hco/2/GRCh38#95852521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118495590-C-A

http://identifiers.org/hco/2/GRCh38#95853201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118498231-C-A

95853282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498316-G-A

95853282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498316-G-T

95853353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498382-T-C

95853355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498384-G-A

95853355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498384-G-C

95853355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498384-G-T

95853412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498398-A-G

95853463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118498449-T-A

http://identifiers.org/hco/2/GRCh38#95853470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118498456-A-C

95853829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118498922-A-G

95855255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118499889-T-G

95855281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118499915-C-G

95855341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118499975-A-G

http://identifiers.org/hco/2/GRCh38#95855380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500014-A-C

95855380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118500014-A-G

95855397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118500031-C-G

http://identifiers.org/hco/2/GRCh38#95855488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500122-C-A

95855488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118500122-C-T

95855733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118500400-C-G

95855733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118500400-C-T

95855776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118500443-T-C

95856674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501311-A-G

95856769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501402-C-T

http://identifiers.org/hco/2/GRCh38#95857261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118502635-A-C

95857261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502635-A-G

95857381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118502766-C-T

95857405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118502790-C-T

95857406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118502791-T-C

95857430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118502815-C-G

http://identifiers.org/hco/2/GRCh38#95857446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118502831-A-C

95857446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118502831-A-G

95857446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118502831-A-T

95857500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118502889-T-A

95858476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118503094-T-C

95858510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118503128-G-C

95859909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118504665-T-A

95859909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118504665-T-C

95859926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118504682-T-A

95859926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118504682-T-C

http://identifiers.org/hco/2/GRCh38#95859975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118504731-C-A

95859975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118504731-C-T

95860019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118504775-T-G

http://identifiers.org/hco/2/GRCh38#95860046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118504802-C-A

http://identifiers.org/hco/2/GRCh38#95860184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118504908-C-A

95860184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118504908-C-T

http://identifiers.org/hco/2/GRCh38#95860196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118504920-C-A

95860197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118504921-T-A

95860197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118504921-T-C

http://identifiers.org/hco/2/GRCh38#95860332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118505044-A-C

95860432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118505107-A-G

http://identifiers.org/hco/2/GRCh38#95877501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517136-C-A

95877501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517136-C-T

http://identifiers.org/hco/2/GRCh38#95877528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517161-C-A

95877528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517161-C-G

http://identifiers.org/hco/2/GRCh38#95877605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517231-C-A

95882421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118516767-A-G

95882479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118516818-G-A

95882501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118516840-A-G

95882501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118516840-A-T

http://identifiers.org/hco/2/GRCh38#95882586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516924-C-A

95882848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517184-G-T

95883094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-T-C

95883140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517471-G-T

95884963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-T-C

95888432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517149-A-G

95888514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517227-A-G

95888603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517313-T-C

95888711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-T-C

95888757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517471-T-G

95890475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517313-T-C

95892261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517231-C-T

95892361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517328-T-C

95892455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-T-C

http://identifiers.org/hco/2/GRCh38#95894319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517425-A-C

95894319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-A-G

95894319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-A-T

95895738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118516982-G-A

95895738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118516982-G-C

95895738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118516982-G-T

95895939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517184-G-A

95895988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517227-A-G

95895992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517231-C-T

95897966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517328-T-A

95898021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517384-T-A

95898060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-T-C

95903582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517328-T-A

95903646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517393-T-C

95903676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118517425-C-T

95909292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-C-G

95909292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-C-T

95916572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517231-C-G

95919756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 118516670-T-A

95919756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 118516670-T-C

95919756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 118516670-T-G

95919827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516745-A-G

95919846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516767-A-G

95919852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516773-T-C

95920317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517227-A-G

95920406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517313-T-C

95920477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517384-T-C

95920486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517393-T-A

95922366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517384-T-C

95922405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-C-T

95925471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516767-A-G

95925529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118516818-G-A

95925529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 118516818-G-T

http://identifiers.org/hco/2/GRCh38#95925551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516840-A-C

95925629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-G-A

95925629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-G-T

http://identifiers.org/hco/2/GRCh38#95925636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516924-C-A

95925636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516924-C-T

95927210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516643-T-C

95927231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118516664-C-T

95927237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118516670-T-C

95927391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118516818-G-A

95927391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 118516818-G-T

95927413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 118516840-A-G

95927491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-A-G

http://identifiers.org/hco/2/GRCh38#95927498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516924-C-A

95927498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516924-C-G

95927989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-T-G

95941127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118525848-G-A

95941127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118525848-G-C

95941127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118525848-G-T

95941140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118525861-A-G

95941140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118525861-A-T

95941158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 118525879-A-G

95941167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 118525888-T-C

95941170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 118525891-T-C

95941183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118525904-G-A

95941183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118525904-G-C

95941183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118525904-G-T

95941184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118525905-G-A

95941184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118525905-G-C

95941184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118525905-G-T

95941204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 118525925-T-A

http://identifiers.org/hco/2/GRCh38#95944595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118526398-C-A

95944598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118526401-T-C

95944636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 118526443-A-G

http://identifiers.org/hco/2/GRCh38#95944651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118526458-C-A

95945206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118526689-A-G

95945266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118526745-G-A

95945266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118526745-G-T

95945427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118526890-C-T

95945562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527011-A-G

95945586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527033-G-A

95945586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527033-G-C

95945615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527068-T-C

95945615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527068-T-G

95945693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527145-C-T

95945711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118527161-G-A

95947965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528408-T-A

http://identifiers.org/hco/2/GRCh38#95947998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118528438-C-A

95948247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528687-G-C

95948247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528687-G-T

95948263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528703-G-A

95948263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528703-G-C

95948269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528709-C-T

95948408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528837-A-G

95948413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118528842-A-T

95948578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 118528984-G-A

95948578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118528984-G-T

95948586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118528992-G-C

95948586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118528992-G-T

95948627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529037-G-T

95948704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529250-A-G

95948713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529259-G-A

95948713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529259-G-T

95948717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529263-G-A

95948717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529263-G-C

95948717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529263-G-T

http://identifiers.org/hco/2/GRCh38#95948719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118529265-C-A

95948742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529285-A-G

95948773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118529319-T-C

http://identifiers.org/hco/2/GRCh38#95957308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517231-C-A

95957463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517384-T-C

95957472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517393-T-C

95957502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-T-C

95957879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517774-G-C

95957913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517801-T-C

95957973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517853-T-C

95957977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517857-C-T

95957994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517875-A-T

95958587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516643-T-C

95958608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118516664-T-C

http://identifiers.org/hco/2/GRCh38#95958683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516745-A-C

95958710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516767-A-G

95958767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118516818-G-A

95958867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-G-C

95958867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-G-T

95958901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516955-G-T

95959088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517136-C-T

95959101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517149-A-G

95959113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517161-A-G

95959113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517161-A-T

http://identifiers.org/hco/2/GRCh38#95959185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517227-A-C

95959289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517328-C-T

95959383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-T-C

95959543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517567-T-C

95959562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517584-G-C

95959787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517793-A-G

95959795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517801-T-A

95959795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517801-T-C

95959855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517853-T-C

http://identifiers.org/hco/2/GRCh38#95959859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517857-C-A

95959876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517875-A-G

95959876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517875-A-T

95960469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516643-T-C

95960490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118516664-T-C

95960598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516773-T-C

95960649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 118516818-G-A

95960749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-G-C

95960749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516917-G-T

95960756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118516924-C-T

95960995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517161-A-G

95961156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517313-T-C

95961171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517328-C-T

95961265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517425-T-C

95961425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517567-T-A

95961599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517733-T-C

95961643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517774-G-T

95961669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517793-A-G

95961677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118517801-T-C

95990180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118537706-T-G

http://identifiers.org/hco/2/GRCh38#95990225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118537751-C-A

95990433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538084-G-T

95990501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538152-T-G

95990573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538199-G-A

95991218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538677-C-T

95991455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538719-G-A

95991455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538719-G-T

http://identifiers.org/hco/2/GRCh38#95991458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538722-C-A

95991474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538734-G-A

95991474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538734-G-C

95991474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538734-G-T

http://identifiers.org/hco/2/GRCh38#95991490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538750-C-A

95991490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32946
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 118538750-C-T