108134557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3 prime UTR variant
orthologous variants: 109076255-G-T

108134659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3 prime UTR variant
orthologous variants: 109076166-C-T

108134909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109075686-T-C

108135270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109075325-T-C

108135329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109075271-T-A

108135329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109075271-T-C

108135498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074927-A-T

108135643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074809-T-C

108135749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074701-A-T

108135838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074619-A-G

108135933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074532-T-C

108136054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074420-T-C

http://identifiers.org/hco/1/GRCh38#108136058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109074416-C-A

108136099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074374-C-T

108136141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074335-G-A

108136141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074335-G-T

http://identifiers.org/hco/1/GRCh38#108136149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109074327-C-A

108136149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074327-C-T

108136181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074318-G-T

http://identifiers.org/hco/1/GRCh38#108136309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109074150-C-A

108136309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074150-C-G

http://identifiers.org/hco/1/GRCh38#108136345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109074114-C-A

108136345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074114-C-G

108136345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074114-C-T

108136433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109074033-A-T

108136507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073962-G-C

108136507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073962-G-T

http://identifiers.org/hco/1/GRCh38#108136520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109073949-A-C

108136520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073949-A-G

108136540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073929-T-C

108136567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073904-A-G

108136581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073890-A-G

108136583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073888-T-G

108136610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073869-T-G

108136611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 109073868-G-T

108136830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 109073647-T-C

108136852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073609-A-T

108136878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073561-G-A

108136878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073561-G-C

108136878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073561-G-T

http://identifiers.org/hco/1/GRCh38#108136900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109073539-C-A

108136900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073539-C-T

108136917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073521-G-T

108136928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073512-A-G

108136946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073494-A-G

http://identifiers.org/hco/1/GRCh38#108137105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109073370-A-C

108137198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073300-G-A

108137374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109073164-T-G

108137673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109072310-C-G

108137724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109072246-G-A

108138342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109071768-A-T

108138382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109071722-T-C

108138385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109071719-A-G

108138515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109071597-G-A

108138565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109071551-T-A

108138937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070975-A-G

108138937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070975-A-T

108138943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070969-G-A

108138943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070969-G-C

108138943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070969-G-T

108138946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070966-T-G

108138947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070965-G-T

http://identifiers.org/hco/1/GRCh38#108138951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109070961-A-C

108138953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070959-T-C

108139165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109070776-A-G

108139257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070676-A-G

108139257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109070676-A-T

108143544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 109068697-T-C

108143547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109068694-T-C

http://identifiers.org/hco/1/GRCh38#108143728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109068509-C-A

108143850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068408-T-C

108143852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068406-T-C

http://identifiers.org/hco/1/GRCh38#108143853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109068405-C-A

108143853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068405-C-T

108143854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068404-A-G

108143889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068369-C-T

108143936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068324-A-G

108144022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068243-T-A

108144049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109068219-C-T

108144164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067771-T-C

108144198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067737-T-C

108147732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067327-A-G

108147744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067307-G-A

108147744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067307-G-T

108147909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067138-C-T

http://identifiers.org/hco/1/GRCh38#108148010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109067043-C-A

108148010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109067043-C-T

108148072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066956-C-T

108148081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066948-A-T

108148097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066932-T-G

108148138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066897-T-C

108148138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066897-T-G

108148177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066868-A-G

108148183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066862-T-C

108148226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066820-T-C

108148231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066815-A-T

108148254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066792-A-G

108148367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109066681-T-G

108148398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066613-A-G

108148399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066612-G-T

108148506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066504-T-C

108148568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066447-G-T

108148667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066367-A-G

108148858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066210-T-C

108148871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066197-G-A

108148881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109066187-C-T

http://identifiers.org/hco/1/GRCh38#108154964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109065977-C-A

108154964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109065977-C-T

108154990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109065951-T-C

108155014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109065927-T-C

108155158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109065789-A-G

108156425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109065450-C-G

http://identifiers.org/hco/1/GRCh38#108156651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109065216-A-C

108156665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109065148-A-G

108156762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109064930-A-G

108157024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109064675-A-T

http://identifiers.org/hco/1/GRCh38#108157318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109064378-A-C

108157318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109064378-A-G

108157430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109064333-G-T

108157510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 109064271-G-C

108157517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109064264-C-T

108157630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109064151-T-A

108157630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109064151-T-C

108158333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063949-T-C

108158333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063949-T-G

108158606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063756-G-A

108159066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063630-T-C

108159089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063606-A-T

108159442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063249-G-T

108160985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063227-G-A

108160985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109063227-G-C

http://identifiers.org/hco/1/GRCh38#108161080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109063141-C-A

108161118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109062473-T-C

108161119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109062472-G-T

108161129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109062462-T-C

108161228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109062373-G-C

108161228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 109062373-G-T

108161295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 109062306-T-C

108161329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109062272-A-G

108161354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109062241-T-C

http://identifiers.org/hco/1/GRCh38#108161392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109062203-A-C

108161538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109061936-C-T

108180929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109060450-T-C

108181801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109057027-T-A

108181801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109057027-T-C

108181801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109057027-T-G

108181867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056962-A-G

108181867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056962-A-T

108181872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056957-T-C

108181922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056905-A-G

108181924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056903-C-T

108182167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056701-T-A

108182167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056701-T-C

108182167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056701-T-G

108182194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056675-T-C

108182361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056433-T-C

108182465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056240-T-G

108183016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109056041-T-C

108183985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109045318-G-C

108184301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109045030-G-A

108184389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109044933-A-G

108184440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109044882-G-A

108184460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109044859-A-G

108185316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109044279-C-T

108185421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109044189-T-G

108185635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043991-A-T

http://identifiers.org/hco/1/GRCh38#108185666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109043921-A-C

108185839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 109043641-T-G

http://identifiers.org/hco/1/GRCh38#108185860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109043620-A-C

108185860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 109043620-A-T

108185914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 109043566-A-G

108185957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 109043523-A-G

108185957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 109043523-A-T

108185993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043478-G-A

108185993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043478-G-T

108186027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043444-A-G

108186041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043430-T-C

108186064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043408-T-C

108190124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043202-C-G

108190132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043194-T-C

108190229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043098-G-C

108190238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109043089-T-C

108190323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042995-G-A

108190342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042976-G-T

http://identifiers.org/hco/1/GRCh38#108190428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109042866-C-A

108190518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042815-T-C

108190530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042803-C-G

108190662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042647-G-T

108190796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042362-C-T

108190912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109042248-C-T

108191608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109041844-A-G

108192549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041101-G-A

108192549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041101-G-C

108192554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041096-A-G

108192590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041060-T-A

108192590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041060-T-C

108192605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041051-C-G

108192606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041050-C-G

108192606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 109041050-C-T

108192623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109041033-G-A

108192623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109041033-G-T

108192625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109041031-G-A

108192625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109041031-G-T

http://identifiers.org/hco/1/GRCh38#108192763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109040911-C-A

108192763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040911-C-T

http://identifiers.org/hco/1/GRCh38#108192796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109040878-A-C

108192796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040878-A-G

108192814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040862-G-A

108192814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040862-G-C

108192814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040862-G-T

108192835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040838-C-G

108192835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109040838-C-T

108192846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109040829-C-T

108192872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109040805-G-T

108192887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109040796-C-T

http://identifiers.org/hco/1/GRCh38#108192888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109040795-C-A

108192888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109040795-C-T

http://identifiers.org/hco/1/GRCh38#108192961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109040749-A-C

108194185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109039695-G-C

108194238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109039642-C-T

108197213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109036965-T-A

108197349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109036655-G-A

http://identifiers.org/hco/1/GRCh38#108197454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109036556-C-A

108197671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109036327-T-A

108197682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 109036316-G-A

108198990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109031514-T-C

108199152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109031376-T-A

108199324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031192-G-A

108199324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031192-G-T

108199394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031127-T-C

108199394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031127-T-G

http://identifiers.org/hco/1/GRCh38#108199464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109031059-A-C

108199464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031059-A-G

108199482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031045-T-A

108199482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031045-T-C

108199482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109031045-T-G

108199600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109030968-A-G

http://identifiers.org/hco/1/GRCh38#108199631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030940-A-C

108199687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109030885-T-A

108199687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 109030885-T-G

108199708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030881-G-C

108199758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030834-A-G

http://identifiers.org/hco/1/GRCh38#108199767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030830-C-A

108199839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030796-A-T

http://identifiers.org/hco/1/GRCh38#108199906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030739-A-C

108199906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030739-A-G

108199906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030739-A-T

108199913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030732-G-A

108199913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 109030732-G-T

http://identifiers.org/hco/1/GRCh38#108199941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030716-C-A

108199941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 109030716-C-T

108199963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 109030694-G-A

108199963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 109030694-G-T

108200071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 109030586-C-T

108200074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 109030583-G-T

108200111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 109030546-G-A

108200111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 109030546-G-T

108200141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030516-T-G

108200224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030464-G-A

108200224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030464-G-C

http://identifiers.org/hco/1/GRCh38#108200244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030445-C-A

108200244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030445-C-G

http://identifiers.org/hco/1/GRCh38#108200246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030443-A-C

108200246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030443-A-G

108200252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030437-T-A

108200252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030437-T-C

http://identifiers.org/hco/1/GRCh38#108200312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030363-C-A

108200312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030363-C-G

108200312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 109030363-C-T

108200397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030290-G-A

108200397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030290-G-T

108200459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030225-T-A

108200459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030225-T-C

108200459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030225-T-G

108200466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030218-A-G

108200474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030209-T-A

108200474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030209-T-C

http://identifiers.org/hco/1/GRCh38#108200614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#109030109-C-A

108200633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030089-G-A

108200633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030089-G-T

108200719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030053-T-C

108200719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030053-T-G

108200754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20662
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 109030039-A-G