39105846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6694681-T-C

39106101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693948-A-T

39106281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693779-T-C

39106366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693710-A-G

39106369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693707-A-G

39106413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693664-T-C

http://identifiers.org/hco/5/GRCh38#39106550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6693534-A-C

http://identifiers.org/hco/5/GRCh38#39106618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6693471-C-A

39106618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693471-C-T

http://identifiers.org/hco/5/GRCh38#39106854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6693244-C-A

39106897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693201-A-G

39106901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3 prime UTR variant
orthologous variants: 6693197-T-G

39107127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6693072-T-A

http://identifiers.org/hco/5/GRCh38#39107231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6692915-C-A

39107231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692915-C-G

39107231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692915-C-T

39107237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692909-T-A

39107237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692909-T-C

39107237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692909-T-G

39107276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692794-T-C

39107276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6692794-T-G

39107363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692724-G-A

39107363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692724-G-C

39107363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692724-G-T

39107416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692678-A-G

http://identifiers.org/hco/5/GRCh38#39107419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6692675-C-A

39107419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692675-C-G

39107419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692675-C-T

39107435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692659-G-A

39107435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692659-G-C

39107435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 6692659-G-T

39107604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6691829-G-A

39107604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6691829-G-T

39107608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6691825-T-C

39107774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6691275-A-G

39107914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690856-T-C

39107970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690606-C-T

39108063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690339-C-T

http://identifiers.org/hco/5/GRCh38#39108085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6690312-C-A

39108085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690312-C-T

39108089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690308-G-A

39108089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690308-G-T

39108160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690238-T-C

39108168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690236-G-T

39108264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 6690160-T-A

39108264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 6690160-T-C

http://identifiers.org/hco/5/GRCh38#39108348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6690081-A-C

39108348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690081-A-G

39108351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6690078-T-G

39108533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689869-T-C

39108562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689818-A-G

39108758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689618-G-A

http://identifiers.org/hco/5/GRCh38#39108985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6689418-C-A

39109100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689310-G-T

39109206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689204-C-T

39109210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689200-A-G

39109399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6689027-T-A

39109563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688812-T-C

39109614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688760-C-T

39109618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688756-T-G

39109644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688731-T-C

39109680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688699-A-G

39109903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688471-G-C

http://identifiers.org/hco/5/GRCh38#39109968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6688407-C-A

39109968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688407-C-T

39110059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688314-T-C

39110154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688228-G-A

39110171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688213-G-A

39110260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688136-A-G

39110275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6688121-T-C

39110401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6687999-A-G

http://identifiers.org/hco/5/GRCh38#39110427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6687938-C-A

39110427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6687938-C-T

39112493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6687044-T-C

39112979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6686452-G-A

39113112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6686328-G-A

39113424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6686030-A-G

http://identifiers.org/hco/5/GRCh38#39118743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6682126-C-A

39118798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6682081-T-C

39118809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6682070-T-G

39118838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6682057-A-G

39118844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6682051-G-A

39118844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6682051-G-T

39118897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6682000-A-G

39118900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681997-A-G

39118990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681907-G-A

39118990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681907-G-C

39118990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681907-G-T

39118993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681904-G-A

39118993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681904-G-C

39118993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681904-G-T

http://identifiers.org/hco/5/GRCh38#39119018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6681879-C-A

39119018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6681879-C-T

39119038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 6681859-T-A

39119038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 6681859-T-C

39119049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681848-G-A

39119049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681848-G-C

39119049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681848-G-T

39119094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681809-T-A

39119104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681803-T-C

39119110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681797-T-C

39119502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681414-T-C

39119638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6681279-G-T

39119676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681245-A-G

http://identifiers.org/hco/5/GRCh38#39119739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6681174-C-A

39119739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681174-C-T

http://identifiers.org/hco/5/GRCh38#39119764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6681017-C-A

39119764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6681017-C-T

http://identifiers.org/hco/5/GRCh38#39119867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6680924-C-A

39119952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6680867-C-T

http://identifiers.org/hco/5/GRCh38#39120136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6680692-A-C

39120693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6680382-A-G

39120894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6680184-T-C

39121096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679986-G-A

39121140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679941-C-T

39121173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679901-T-A

39121175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679899-A-T

http://identifiers.org/hco/5/GRCh38#39121232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6679862-C-A

http://identifiers.org/hco/5/GRCh38#39121262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6679823-C-A

39121302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679784-A-T

39121412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679682-A-G

39121482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679631-A-G

39121486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679627-T-C

39121532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679542-T-C

39121668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679127-C-T

39121688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6679107-T-G

39121972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678761-A-T

39122001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678732-A-T

39122014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678719-G-A

39122029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678705-A-G

39122187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678549-A-G

http://identifiers.org/hco/5/GRCh38#39122254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6678481-C-A

39122254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678481-C-T

http://identifiers.org/hco/5/GRCh38#39122434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6678301-C-A

39122434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678301-C-T

http://identifiers.org/hco/5/GRCh38#39122465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6678270-C-A

39122465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678270-C-G

39122470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678265-A-G

39122470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678265-A-T

39122630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6678067-T-C

39124095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6676300-C-T

39124179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6676214-A-G

39124179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6676214-A-T

http://identifiers.org/hco/5/GRCh38#39124283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6676111-A-C

39124283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6676111-A-G

39124283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6676111-A-T

39124307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6676078-A-G

39124398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675993-T-A

39124398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675993-T-C

39124426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675965-T-C

39124538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675861-G-A

39124710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675692-G-A

39124736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675665-C-T

39124822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675578-T-A

39124822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675578-T-C

39124849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675552-G-A

39124914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675493-T-C

39124915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675481-C-G

39124988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675362-G-T

39125291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6675061-C-G

39125468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6674912-A-T

http://identifiers.org/hco/5/GRCh38#39125884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6674492-A-C

39125884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6674492-A-T

http://identifiers.org/hco/5/GRCh38#39125946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6674430-A-C

39126243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6674139-T-A

39127376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6673526-T-C

39127688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 6673295-A-T

39127743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 6673240-A-G

39127743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 6673240-A-T

39127744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 6673239-T-A

39127902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6673078-T-G

39127921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6673059-T-C

39127921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6673059-T-G

http://identifiers.org/hco/5/GRCh38#39130607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6672041-C-A

39130607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6672041-C-T

39130619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6672029-A-G

39130650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671995-A-G

39130650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671995-A-T

39130656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671989-T-C

39130740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671912-T-C

39130971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671703-C-T

39131512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671217-G-A

39131583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671151-T-C

39131748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6671042-A-G

http://identifiers.org/hco/5/GRCh38#39131792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6670998-A-C

39131794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670996-C-G

39131825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670970-G-A

http://identifiers.org/hco/5/GRCh38#39133636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6670709-C-A

39133680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670665-T-C

39133680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670665-T-G

http://identifiers.org/hco/5/GRCh38#39133889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6670384-C-A

39133936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670337-C-T

39133956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670317-A-T

39134104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6670166-G-T

39134220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6670052-T-A

39134731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6669275-T-C

39134796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668494-A-G

39134811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668481-T-C

39134844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668456-T-C

39135007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6668293-C-T

39135027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668273-A-G

39135035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668265-T-C

39135085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668239-G-T

39135096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668227-G-A

39135096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668227-G-T

39135103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6668220-A-G

39135841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6666325-A-G

39135841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6666325-A-T

39135889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6666288-T-C

39136498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6665338-A-G

39137051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6664776-G-C

39137218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6664633-G-A

http://identifiers.org/hco/5/GRCh38#39137346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6664551-A-C

http://identifiers.org/hco/5/GRCh38#39137380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6664518-C-A

39137380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6664518-C-T

39137587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6664408-A-T

39137715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6664280-G-A

http://identifiers.org/hco/5/GRCh38#39137779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#6664216-C-A

39137780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6664215-C-T

http://identifiers.org/hco/5/GRCh38#39137927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#6664063-C-A

39137947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6664043-T-C

39137964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6664026-G-A

39137964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6664026-G-T

39137996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6663998-A-G

39137999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6663995-T-C

39138026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6663981-T-C

39138064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6663951-G-A

39138064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6663951-G-T

39138426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662492-G-C

39138426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662492-G-T

http://identifiers.org/hco/5/GRCh38#39138446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6662478-C-A

39138639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662308-A-G

39138701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662246-A-G

39138723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662229-T-C

http://identifiers.org/hco/5/GRCh38#39138806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6662164-C-A

39138806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662164-C-G

39138806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662164-C-T

39138924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6662089-A-G

39138953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6662042-T-C

http://identifiers.org/hco/5/GRCh38#39139030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6661969-C-A

39139042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661955-A-G

39139059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661938-T-C

39139070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661927-T-A

39139070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661927-T-C

39139132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661862-G-T

39139154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661841-A-G

39139159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661836-T-C

39139183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661812-G-A

39139183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661812-G-C

39139183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661812-G-T

http://identifiers.org/hco/5/GRCh38#39139246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#6661750-C-A

39139246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661750-C-G

39139246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6661750-C-T

39139548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6661450-G-A

39139548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6661450-G-T

http://identifiers.org/hco/5/GRCh38#39139570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6661412-A-C

39139572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6661410-G-A

39139572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6661410-G-T

http://identifiers.org/hco/5/GRCh38#39139616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6661359-C-A

39139813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6661158-G-A

http://identifiers.org/hco/5/GRCh38#39140627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6660027-C-A

39140636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6660018-G-A

39140709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6659961-G-A

39140753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6659917-A-G

39140826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6659848-A-G

http://identifiers.org/hco/5/GRCh38#39140980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6659712-C-A

39140980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6659712-C-T

39141055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6659636-G-C

39141055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6659636-G-T

39146666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6656901-G-A

39146738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6656842-G-T

39146754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6656837-T-G

http://identifiers.org/hco/5/GRCh38#39146789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6656805-A-C

39148391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6656049-T-G

39148417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6656015-T-A

39148460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655983-T-C

39148464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655979-T-A

39149076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655451-T-A

39149076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655451-T-C

39149142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655380-G-C

39149170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655350-A-G

39149200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6655319-T-C

39149219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655301-C-T

39149303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655223-C-T

39149330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655195-C-G

39149498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6655025-T-C

39150720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6654541-T-C

39150771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6654485-C-T

39151000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6654278-A-G

39151082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6654154-A-G

39151727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6653676-G-A

39151899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6653547-C-T

39151934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6653525-G-C

39151995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6653465-C-T

39151996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6653464-T-C

39152061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6653409-G-A

http://identifiers.org/hco/5/GRCh38#39153350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6649327-A-C

39153350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6649327-A-G

39153350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6649327-A-T

39153405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6649272-G-T

http://identifiers.org/hco/5/GRCh38#39153426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6649251-C-A

39153426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6649251-C-T

39153454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6649223-T-C

39153463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6649214-G-A

39153463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6649214-G-C

39153463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6649214-G-T

39153577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6649100-G-A

39155998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6646216-C-T

39156274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645935-G-A

39156274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645935-G-C

39156313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645896-A-T

39156352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645858-G-T

39156439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645773-G-C

http://identifiers.org/hco/5/GRCh38#39156462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6645747-A-C

39156518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645695-T-C

39156706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645097-A-G

39156709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6645094-G-A

39157179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644629-T-A

39157245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644572-A-G

39157332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644483-G-A

39157445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644384-T-C

39157499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644333-C-G

39157499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644333-C-T

39157513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644320-A-G

39157594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644248-A-T

http://identifiers.org/hco/5/GRCh38#39157643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6644202-C-A

39157643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6644202-C-T

39160937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6642882-C-G

39162144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6643473-C-T

39162973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6642769-T-G

http://identifiers.org/hco/5/GRCh38#39163174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6642585-C-A

39163202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6642557-A-G

39163849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6641162-T-G

39164090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6640099-T-G

39164791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6638535-G-A

39164903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6638428-A-G

39164951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6638380-T-C

39164992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6638340-G-A

39166980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6638194-C-T

39166983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6638191-G-A

39171815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6634571-G-C

39171863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6634525-G-A

39171958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6634434-G-A

39174565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6634084-C-T

39174617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6634036-T-G

http://identifiers.org/hco/5/GRCh38#39174788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6633863-A-C

39174951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633717-G-A

39175041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633632-G-A

39175104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633583-G-A

39175104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633583-G-T

39175644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633155-C-T

39175657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633142-A-T

39175673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6633129-C-G

39175888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6632624-C-T

39175898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6632613-G-A

39176025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6632496-C-G

39176512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6632338-A-G

http://identifiers.org/hco/5/GRCh38#39176677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6632177-A-C

39176932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6631914-A-G

39177073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6631825-G-T

39177248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6631653-T-C

39178069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6630818-C-T

39179173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6628268-T-C

39179232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6627262-C-T

http://identifiers.org/hco/5/GRCh38#39179291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6627219-A-C

39179383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6627125-A-G

39180134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6626360-A-G

39180306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6626183-C-G

39180603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625935-A-G

39180633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625905-T-C

39180657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625885-C-T

39180719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625831-A-G

39180815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625752-T-C

39180851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625711-G-C

39180858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625704-T-A

39181056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625540-T-C

39181101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625506-T-C

39181130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625478-G-C

39181144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625464-C-G

http://identifiers.org/hco/5/GRCh38#39183464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6625047-A-C

39183496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6625017-A-G

39183633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6624885-C-T

http://identifiers.org/hco/5/GRCh38#39183643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6624872-A-C

39183643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6624872-A-G

39183646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6624869-T-C

39183808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6624529-G-A

39183942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6624429-G-T

39184357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6624028-G-A

39184472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6623917-A-T

http://identifiers.org/hco/5/GRCh38#39185498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6622810-A-C

39185498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622810-A-G

http://identifiers.org/hco/5/GRCh38#39185511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6622797-C-A

39185511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622797-C-T

39185590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622774-A-G

http://identifiers.org/hco/5/GRCh38#39185627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6622737-C-A

39185627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622737-C-T

39186919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622598-A-G

39186957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622561-T-C

39187227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622303-C-T

39187298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6622232-G-A

39187365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6622165-T-G

39187399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6622131-G-A

39187544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621984-T-C

39187545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621983-T-C

39187561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621969-T-C

39187582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621949-T-C

39187596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621936-C-T

39187630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621911-G-A

39187747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621801-G-A

39187779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621769-C-G

39187794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621755-C-T

39187799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621750-A-T

39187891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621564-T-C

39187891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621564-T-G

39187914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621540-A-G

39188149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621330-T-C

39188333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621179-G-A

39188333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621179-G-C

39188420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621083-T-A

39188420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6621083-T-C

39189048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6620799-C-G

39189235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6620704-C-T

39189256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6620683-A-G

39189256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6620683-A-T

39189271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6620667-G-A

39189271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6620667-G-T

39190024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6618993-A-G

http://identifiers.org/hco/5/GRCh38#39190103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6618918-C-A

39190180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6618848-A-G

http://identifiers.org/hco/5/GRCh38#39190694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6618577-C-A

39190791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6618522-T-A

39191327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617893-G-A

39191685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617544-C-T

39191918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617307-T-C

39192076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617136-G-T

39192116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617096-A-G

39192168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617043-G-A

39192168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6617043-G-C

39192717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616407-T-C

39192742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616385-T-C

39192783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616347-G-C

http://identifiers.org/hco/5/GRCh38#39192866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6616269-A-C

http://identifiers.org/hco/5/GRCh38#39192892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6616245-C-A

39192892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616245-C-T

39192916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616231-G-A

39193101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616113-G-T

39193216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6616005-A-G

39193409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6615829-G-T

39193605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6615632-G-A

39193621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6615616-A-G

39194357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6615047-C-T

39194375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6615029-C-T

39194902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6614755-G-A

39195019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6614637-G-A

39195024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6614632-C-T

39195905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6613497-A-T

39195940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6613456-T-C

http://identifiers.org/hco/5/GRCh38#39196141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6613268-A-C

39196356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6613209-A-T

39196518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6613192-G-T

39197514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6612287-A-G

39197515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6612286-T-C

http://identifiers.org/hco/5/GRCh38#39197521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6612280-C-A

39200826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6611580-G-A

39200997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6611371-T-A

39201136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6611182-A-G

39201242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6611075-C-G

39201478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6610887-A-T

39201483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6610884-G-A

http://identifiers.org/hco/5/GRCh38#39201654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6610695-C-A

39201662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6610687-G-T

39201704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6610642-T-G

39201754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6610594-T-C

http://identifiers.org/hco/5/GRCh38#39201776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6610574-C-A

39201783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6610567-T-C

39201902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: synonymous variant
orthologous variants: 6610449-C-T

39201915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610436-G-A

39201942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610409-G-A

39202144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610228-G-T

39202269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610109-A-T

39202287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610091-G-T

39202305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610073-A-G

39202317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6610061-G-T

39202467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6609914-T-C

39202488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6609893-G-A

39202728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6609659-G-A

39202728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6609659-G-T

39202819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6609568-G-A

39202917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: missense variant
orthologous variants: 6609470-G-A

39203152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6609222-G-T

39203161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6609213-G-A

39203161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6609213-G-T

39203257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6609121-C-T

39203306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6609075-T-C

http://identifiers.org/hco/5/GRCh38#39203421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6608966-C-A

http://identifiers.org/hco/5/GRCh38#39203588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6608811-A-C

39203588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6608811-A-G

39203674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6608726-T-A

39203929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6608493-C-T

39205220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607815-A-G

39205400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607691-C-T

39205414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607683-T-A

39205431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607670-T-C

39205779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607339-G-A

39205877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607253-C-T

39205908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6607217-A-T

http://identifiers.org/hco/5/GRCh38#39206035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6607010-A-C

39208135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6605786-T-C

39208149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6605766-T-G

39208517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6605430-G-A

http://identifiers.org/hco/5/GRCh38#39208994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6604983-C-A

39209111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604824-T-C

39209260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604686-T-A

39209260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604686-T-C

39209616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604627-A-G

39209929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604354-A-T

39210032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604251-C-T

39210036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604247-C-T

39210085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604201-G-A

http://identifiers.org/hco/5/GRCh38#39210202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6604089-C-A

39210202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604089-C-T

http://identifiers.org/hco/5/GRCh38#39210209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6604082-C-A

39210269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6604019-G-A

39210313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6603973-C-T

http://identifiers.org/hco/5/GRCh38#39210525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6603760-A-C

39210637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6603653-T-A

39211083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 6603344-C-T

39211161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6603266-G-T

39211178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6603249-A-G

39211727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6603044-G-A

39211782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6602994-C-G

39211908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6602895-G-A

39216625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6602122-T-C

39216638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6602109-G-A

39216682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6602065-C-T

39216802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601975-G-T

http://identifiers.org/hco/5/GRCh38#39216849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6601932-C-A

39217093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601327-G-A

39217093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601327-G-T

39217137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601290-C-T

39217147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601278-A-G

39217175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601253-T-G

39217218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6601208-C-T

39217443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6600994-T-C

http://identifiers.org/hco/5/GRCh38#39217675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6600826-A-C

39217845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6600673-C-T

39217982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6600541-C-T

39218140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6600422-A-G

http://identifiers.org/hco/5/GRCh38#39218325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6600255-C-A

39218400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6600154-C-T

39218841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599704-T-G

http://identifiers.org/hco/5/GRCh38#39218899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6599645-C-A

39219224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599341-C-T

39219312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599275-A-G

39219312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599275-A-T

39219320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599267-T-C

39219321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599266-G-A

39219321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599266-G-T

39219378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599211-G-A

39219382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599207-T-C

39219384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599205-T-A

39219384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599205-T-C

39219434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599151-A-G

39219434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599151-A-T

39219498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 6599083-C-T

39219507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 6599074-G-A

http://identifiers.org/hco/5/GRCh38#39219543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6599039-C-A

39219580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6599002-T-C

39219599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598983-T-C

39219604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598978-G-T

39219605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598977-G-T

39219613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598969-A-G

39219881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598708-G-T

39219944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598642-G-A

39220035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598567-G-C

39220103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6598498-T-A

39223695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6597113-G-A

http://identifiers.org/hco/5/GRCh38#39223701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6597107-A-C

39223716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6597093-C-T

39223754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6597055-T-C

39223755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6597054-A-T

39223877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596984-T-C

39223882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596978-C-T

39223948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596929-C-T

39224005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596887-C-T

39224149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596727-T-C

39224221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, undefined
orthologous variants: 6596659-A-G

39224326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596587-C-T

39224386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596535-C-T

39224428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596479-A-G

39224542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596381-A-T

39224558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596361-G-A

39224558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596361-G-C

39224657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596255-G-A

39224738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6596177-T-G

39225841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6594915-A-G

39225956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6594791-A-G

39226250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6594530-A-G

39226415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6594356-A-G

39226468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6594269-C-T

39226539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6594198-T-G

39227312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593633-A-G

39227405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593570-G-A

39227416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593559-T-C

39227456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593514-G-T

39227528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593441-A-G

39227987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593048-A-G

39227988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593047-C-T

39228021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6593022-A-G

http://identifiers.org/hco/5/GRCh38#39228204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6592868-A-C

39228267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6592811-G-A

39230665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6591736-C-T

39230781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6591833-A-G

39232171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6591419-C-T

39232423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6591064-A-G

39233221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6590840-A-T

39233440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6590629-G-A

39233468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6590607-T-C

39233784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6590296-T-C

39233784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6590296-T-G

39234151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6589938-A-G

39234158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6589932-A-G

http://identifiers.org/hco/5/GRCh38#39235134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6589164-C-A

39235137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6589161-G-A

39235164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6589135-G-A

39235296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6589024-C-T

39235511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588822-T-C

39235528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588805-C-G

39235528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588805-C-T

39235595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588740-G-T

39235596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588739-A-T

39235713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588632-A-G

39235729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588619-A-G

39235954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588406-T-C

39236100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588134-A-T

39236208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6588011-G-A

39236839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6587347-G-A

39236926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6587267-C-T

http://identifiers.org/hco/5/GRCh38#39237217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6586991-C-A

39237393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586717-G-A

http://identifiers.org/hco/5/GRCh38#39237460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6586650-C-A

39237542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586575-T-C

39237558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586561-A-G

39237599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586520-C-T

39237722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586283-G-C

39237813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586184-T-C

39237855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586139-T-C

39237879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586115-T-G

39237894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586100-T-C

39237894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586100-T-G

39237933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6586062-G-C

39238140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6585862-A-G

39238207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6585745-T-A

39238207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6585745-T-G

39238260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6585594-T-A

39238326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6585470-T-G

39238651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6585104-G-A

39241486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583849-A-G

39241588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583744-G-A

39241640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583694-C-T

39241664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583672-G-C

39241664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583672-G-T

39241745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583594-A-G

39242039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6583285-A-T

39245331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582940-T-A

39245350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582921-G-T

39245389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582882-G-A

39245389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582882-G-C

39245405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582876-T-C

39245554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582730-G-A

39246327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582176-C-T

39246360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582143-T-C

39246372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582131-T-G

39246397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582120-T-A

39246432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6582103-T-G

39246589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581964-C-T

39246843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581728-C-T

39246862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581702-G-T

39246872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581676-G-A

39246908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581636-T-A

39246963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581582-T-C

39247025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581521-A-G

39247070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581478-T-A

39247070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581478-T-C

http://identifiers.org/hco/5/GRCh38#39247259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6581424-A-C

39247402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6581289-A-G

39247625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6580584-T-G

39247628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6580581-G-C

39247687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6580526-A-G

39247834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6580391-A-T

39247992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6580258-C-T

39248023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6580226-T-C

http://identifiers.org/hco/5/GRCh38#39248142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6578969-C-A

39248186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6578925-A-G

39248189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6578922-G-A

39249019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6578082-C-T

39249179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6577899-G-C

39249186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6577892-C-G

http://identifiers.org/hco/5/GRCh38#39249225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6577851-C-A

39249225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6577851-C-G

http://identifiers.org/hco/5/GRCh38#39249226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6577850-C-A

http://identifiers.org/hco/5/GRCh38#39249311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6577766-A-C

39249311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6577766-A-G

http://identifiers.org/hco/5/GRCh38#39250519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6576701-C-A

39250519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6576701-C-T

39251099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6574900-T-A

39251151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6574848-A-G

39251539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6574506-G-A

39251725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6574327-T-A

39252360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6572997-A-G

39252413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6572944-C-T

39252754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6572422-C-T

39253211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6571995-G-C

39253281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6571950-T-C

39254964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6571322-G-A

39255043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6571242-T-C

39255102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6571202-A-G

39255142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6571150-C-T

39255304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570984-T-C

39255304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570984-T-G

http://identifiers.org/hco/5/GRCh38#39255317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6570971-A-C

39255407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570883-T-C

39255500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570806-C-G

39255826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570468-C-T

39255828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570466-G-C

http://identifiers.org/hco/5/GRCh38#39255973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6570325-C-A

39256002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570304-A-G

39256264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570051-T-A

39256264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6570051-T-C

39256841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6569563-G-A

39256891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6569490-G-A

39257093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6569301-A-T

39257435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6568964-T-C

39262089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564672-A-G

39262151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564607-A-G

http://identifiers.org/hco/5/GRCh38#39262233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6564566-A-C

39262239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564560-C-T

39262617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564233-C-T

39262635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564215-G-A

39262638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564212-C-T

39262721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6564129-A-G

39262951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6563894-G-A

39263122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6563599-G-A

39263122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6563599-G-T

39263134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6563587-C-T

39263643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6556470-A-G

39263682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6556431-T-A

39263768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6556332-C-T

39266689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6555615-A-G

39267299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6554661-A-G

39267515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6554439-T-C

39267519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6554434-T-C

39267533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6554420-A-T

39267958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553981-T-C

39268123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553814-C-T

39269460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553437-G-A

39269499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553395-G-A

39269499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553395-G-C

39269499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553395-G-T

39269520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553373-A-G

39269520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553373-A-T

39269521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553372-G-A

39269521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553372-G-T

39269529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron variant
orthologous variants: 6553364-C-T

39269729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6553218-T-C

39269824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6553121-G-T

39270020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552917-C-T

39270118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552825-A-G

39270254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552693-G-A

39270334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552614-C-T

39270416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552536-C-T

http://identifiers.org/hco/5/GRCh38#39270445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6552506-C-A

39270445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552506-C-T

39270476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552474-A-G

http://identifiers.org/hco/5/GRCh38#39270483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#6552468-A-C

39270483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552468-A-G

39270483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6552468-A-T

39270571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, start_lost
orthologous variants: 6552390-T-C

39270718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552240-G-A

39270718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552240-G-C

39270718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552240-G-T

39270764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552196-G-A

39270786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552173-T-G

39270813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552150-G-T

39270814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552149-A-G

39270814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552149-A-T

39270818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6552145-A-G

39271097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6551735-A-G

39271147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6551687-A-G

39271410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6551381-A-G

39271785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550985-A-G

39271804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550965-T-A

39271804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550965-T-C

39271844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550925-T-A

39271901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550873-G-C

39271922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550856-A-G

39272102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550712-T-G

39272142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550667-A-T

39272178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550631-C-T

39273401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550286-T-A

39273587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6550072-A-G

39273743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549932-G-A

39273743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549932-G-C

39273769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549910-G-A

39273779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549900-A-T

39274341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549734-G-T

39274355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549721-T-A

39274355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549721-T-C

39274392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6549686-T-C

39274462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4036
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6549625-C-T