http://identifiers.org/hco/2/GRCh38#23707932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5129758-C-A

23707998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5129691-G-A

23708235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5129459-A-G

http://identifiers.org/hco/2/GRCh38#23708401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5129292-C-A

23747861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5098182-T-G

23749767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5096290-T-C

http://identifiers.org/hco/2/GRCh38#23749839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5096218-C-A

23749851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5096207-C-T

23750374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5095696-G-A

23750377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5095693-C-T

23750869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5095206-A-G

23750923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5095160-G-C

23750929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5095155-T-C

23750970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5095118-T-C

http://identifiers.org/hco/2/GRCh38#23751159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094927-C-A

23751206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094897-A-T

23751217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094886-T-A

23751217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094886-T-C

23751653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094435-T-C

23751653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094435-T-G

23751654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094434-T-C

http://identifiers.org/hco/2/GRCh38#23751658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094430-C-A

23751658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094430-C-T

23751665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094423-A-G

23751667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094421-A-G

23751674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094414-G-A

23751674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094414-G-T

http://identifiers.org/hco/2/GRCh38#23751683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094406-C-A

23751690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094399-G-C

23751690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094399-G-T

23751704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094385-G-C

23751704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094385-G-T

23751707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094382-G-T

23751708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094381-G-A

http://identifiers.org/hco/2/GRCh38#23751717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094373-C-A

23751717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094373-C-G

http://identifiers.org/hco/2/GRCh38#23751741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094350-A-C

23751741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094350-A-G

23751744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094347-G-A

23751744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094347-G-T

http://identifiers.org/hco/2/GRCh38#23751792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094300-C-A

23751990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094100-G-A

23751990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094100-G-T

23752037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094054-T-A

23752037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5094054-T-C

http://identifiers.org/hco/2/GRCh38#23752047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: http://identifiers.org/mco/12/GRCm39#5094044-C-A

23752047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_retained_variant
orthologous variants: 5094044-C-T

http://identifiers.org/hco/2/GRCh38#23752118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5093975-A-C

23752118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5093975-A-T

23752225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5093871-T-C

23752561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5093617-A-G

23752599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5093570-C-G

23753628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5085000-G-A

23753628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5085000-G-C

23754128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084638-A-G

http://identifiers.org/hco/2/GRCh38#23754129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5084637-A-C

23754129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084637-A-G

23754332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084426-A-G

23754332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084426-A-T

23754421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084339-A-G

23754435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084330-T-C

23754435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5084330-T-G

23754675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5084130-G-A

23754904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5083898-T-C

23755070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5083746-G-A

23756388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5083341-G-A

http://identifiers.org/hco/2/GRCh38#23756493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5083245-C-A

23756572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5083161-A-G

http://identifiers.org/hco/2/GRCh38#23756602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5083127-C-A

23756639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5083010-A-G

23756701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5082811-T-C

23756752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5082767-G-A

23757153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5082391-G-A

23757378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5082215-A-G

http://identifiers.org/hco/2/GRCh38#23757521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5082071-A-C

23757555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 5082037-G-T

23757664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5081925-C-G

23757735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5081854-T-C

23757735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 5081854-T-G

23758068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5081524-T-C

23758086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5081506-T-C

http://identifiers.org/hco/2/GRCh38#23758102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5081490-C-A

23758102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 5081490-C-T

23758289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5081313-G-A

23758375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5081225-A-G

23758427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5081177-C-T

http://identifiers.org/hco/2/GRCh38#23758525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5081069-A-C

23759460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5080565-C-T

23760175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5079729-G-A

23761606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5077743-T-C

23761840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5077516-G-A

23761868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5077505-T-A

23761878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5077495-T-C

23762194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5077193-A-T

23762286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5077101-G-C

23762675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5076730-A-T

23765348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074861-T-C

23765356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074853-T-C

http://identifiers.org/hco/2/GRCh38#23765359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5074849-C-A

23765463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074750-G-A

23765463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074750-G-C

23765463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074750-G-T

http://identifiers.org/hco/2/GRCh38#23765475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5074738-C-A

23765642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074566-T-G

http://identifiers.org/hco/2/GRCh38#23765682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5074526-C-A

23765746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074456-A-G

23766009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5074283-G-A

23766102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5073852-T-A

23766290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5073708-C-G

23776869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5072671-T-C

http://identifiers.org/hco/2/GRCh38#23777061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5072516-A-C

23777090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5072497-G-A

23777498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5072121-T-C

23777512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5072104-C-T

23777632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5071985-T-C

http://identifiers.org/hco/2/GRCh38#23777657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5071966-C-A

23777657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5071966-C-T

23777777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5071852-A-G

23777826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5071801-G-T

23777891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5071736-C-T

23778114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5071309-G-A

23778119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5071304-T-C

23778119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5071304-T-G

23778394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5070992-A-T

23778931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5070599-T-C

23779136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5070416-T-C

23782232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5069016-C-T

23782281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068967-T-C

23782689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068256-T-C

23782723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068222-T-C

23782723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068222-T-G

23782747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068203-A-G

23782759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068191-C-T

23782766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068188-T-A

23782766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068188-T-C

23782780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5068179-T-C

23782892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5068117-T-C

23782904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5068105-T-C

23783279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5067771-G-T

23783328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5067738-A-T

23784070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5067119-G-T

23784536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5065641-T-C

http://identifiers.org/hco/2/GRCh38#23785671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5064339-C-A

23785671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5064339-C-T

http://identifiers.org/hco/2/GRCh38#23785760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5064257-C-A

23785760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5064257-C-T

23786181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5063843-G-A

23786181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5063843-G-T

http://identifiers.org/hco/2/GRCh38#23786256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5063771-A-C

23786256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5063771-A-G

23786256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5063771-A-T

http://identifiers.org/hco/2/GRCh38#23786288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5063733-C-A

23786288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5063733-C-G

23786288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5063733-C-T

23786290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5063731-C-G

23786290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5063731-C-T

http://identifiers.org/hco/2/GRCh38#23788207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5060739-C-A

23788207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060739-C-G

23788263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060660-G-A

23788263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060660-G-T

http://identifiers.org/hco/2/GRCh38#23788265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5060658-C-A

23788265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060658-C-T

http://identifiers.org/hco/2/GRCh38#23788266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5060657-A-C

23788266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060657-A-G

23788267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060656-T-G

23788352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060522-G-A

23788352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5060522-G-T

23788500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5060396-T-C

http://identifiers.org/hco/2/GRCh38#23788725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5060184-C-A

http://identifiers.org/hco/2/GRCh38#23788818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5059745-C-A

23788818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5059745-C-T

23788819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5059744-G-A

23789370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5059338-T-C

23798340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5056592-A-G

23798344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5056588-A-T

http://identifiers.org/hco/2/GRCh38#23798434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5056518-C-A

23798434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5056518-C-T

http://identifiers.org/hco/2/GRCh38#23798476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5056474-C-A

23798944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5055633-C-G

23798970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5055608-A-T

23799300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5055291-C-T

23799810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052344-G-A

23799841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5052327-G-T

23799877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5052298-T-A

23799998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5052184-T-C

23800030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052149-T-C

23800059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5052129-G-A

http://identifiers.org/hco/2/GRCh38#23800267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5051877-A-C

23800341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5051822-C-G

http://identifiers.org/hco/2/GRCh38#23800350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5051813-A-C

23800380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5051786-C-G

23800380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5051786-C-T

23800503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5051661-G-A

23800742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5051542-T-C

23800966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5051365-C-T

23801245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5051009-A-G

23801323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5050809-A-G

http://identifiers.org/hco/2/GRCh38#23801841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5050335-C-A

23801841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5050335-C-G

23801841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5050335-C-T

23802095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5049912-T-G

23802331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5049707-A-G

http://identifiers.org/hco/2/GRCh38#23802501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5049545-A-C

23802501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5049545-A-G

23802719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5049359-C-T

23803052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048620-T-A

23803452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048097-C-G

23803541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048023-G-A

23803719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047841-T-A

23803989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047498-T-C

23804182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047326-A-T

23804228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047280-T-A

23804721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5046804-G-T

23804722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5046803-C-T

23804848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5046688-T-C

http://identifiers.org/hco/2/GRCh38#23808458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5043169-A-C

23808761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5042888-T-G

http://identifiers.org/hco/2/GRCh38#23808849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5042808-A-C

23809106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5042565-A-G

23810234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041107-T-C

23810446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5040926-C-T

23810547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040831-G-A

23812160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5039007-C-G

23812294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5038867-G-A

23813061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5038239-T-G

http://identifiers.org/hco/2/GRCh38#23813890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5036429-A-C

23814026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036322-G-C

23814029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036319-G-A

23814056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036305-T-C

23814056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036305-T-G

23814386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036016-T-A

23814386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036016-T-C

23814457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035953-A-G

23814544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035861-C-T

23815386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035164-T-C

23815431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035096-G-T

23815482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5034994-G-C

http://identifiers.org/hco/2/GRCh38#23815993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5034360-C-A

23816195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5034159-T-C

23816197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5034157-T-G

23816827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5031827-A-G

23817018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5031514-G-C

23817486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5030501-T-C

23817720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5030293-T-C

http://identifiers.org/hco/2/GRCh38#23818334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5029827-C-A

23818338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5029823-C-T

23818388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5029787-T-A

23818388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5029787-T-C

23818409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5029770-A-G

http://identifiers.org/hco/2/GRCh38#23818523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5029656-C-A

23818770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5029190-T-C

http://identifiers.org/hco/2/GRCh38#23819648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5028663-C-A

23819648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028663-C-G

23819728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028605-G-A

23819728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028605-G-T

23819983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028363-T-A

23819983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028363-T-C

23819983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028363-T-G

23819988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028358-A-G

23820227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028149-G-T

http://identifiers.org/hco/2/GRCh38#23820978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5026508-C-A

23820978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5026508-C-T

23821013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5026480-C-T

23821016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5026477-T-C

23821467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5025496-C-T

23821894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024960-T-C

23821896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024958-C-T

23821905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024949-T-C

23821918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024926-C-T

23821945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024870-C-T

23822039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024740-C-G

23822152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024630-C-G

23822152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024630-C-T

23822232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024558-C-T

23823058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024422-G-A

23823108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024392-T-A

23823108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024392-T-C

23823214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5024321-G-A

23823250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5024285-T-G

http://identifiers.org/hco/2/GRCh38#23823278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5024257-C-A

23823518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5024017-G-A

23823594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5023941-G-T

23823629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5023912-G-T

http://identifiers.org/hco/2/GRCh38#23823719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5023848-C-A

23823719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5023848-C-T

23824154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5023582-G-A

23824776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5023258-T-C

23825024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5023083-G-A

http://identifiers.org/hco/2/GRCh38#23825792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5022609-A-C

23825792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022609-A-G

23825932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022464-G-C

23825940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022453-G-A

23825940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022453-G-T

23826219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022197-A-T

23826258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5022147-T-C

23826295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022122-G-A

23826332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022083-T-C

23827001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021263-A-G

23827286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020977-T-C

23827286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020977-T-G

23827330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020938-C-T

23827446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020818-T-C

23827578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020701-A-G

23828701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5019589-A-G

23828960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5019329-A-G

23829058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5019259-T-C

23833887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5016026-A-G

23833887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5016026-A-T

http://identifiers.org/hco/2/GRCh38#23834101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5015811-A-C

23834108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5015800-A-G

23838174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5015385-T-C

23857320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5011402-T-C

23857365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5011357-A-G

23857365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5011357-A-T

http://identifiers.org/hco/2/GRCh38#23857545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5011187-C-A

23857550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5011182-T-C

23862435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5010255-G-A

23862435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5010255-G-T

http://identifiers.org/hco/2/GRCh38#23862499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5010206-C-A

23862542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5010143-T-C

23862606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5010026-T-A

http://identifiers.org/hco/2/GRCh38#23863326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5008285-A-C

23863338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5008273-G-C

23863338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5008273-G-T

http://identifiers.org/hco/2/GRCh38#23863357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5008252-C-A

23863499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5008111-A-G

23863567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5008050-A-G

http://identifiers.org/hco/2/GRCh38#23863568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5008049-A-C

23863613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5008012-A-G

23863614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5008011-A-G

http://identifiers.org/hco/2/GRCh38#23863700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5007926-C-A

23863700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007926-C-T

23863756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007867-A-T

23864703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007723-C-G

23864703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007723-C-T

23864716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007710-T-G

23864724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007697-A-G

23865016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5007357-T-C

http://identifiers.org/hco/2/GRCh38#23865529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5007018-C-A

23865947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5006585-T-C

23866789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5005907-A-G

http://identifiers.org/hco/2/GRCh38#23867110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5005634-A-C

23867145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5005600-A-T

http://identifiers.org/hco/2/GRCh38#23867183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#5005578-C-A

23867459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5005341-C-G

23867642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004837-T-C

23867692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004796-G-A

23867692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004796-G-C

23867692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004796-G-T

23867813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004675-G-T

23867964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004525-G-A

23867964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004525-G-C

23867964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5004525-G-T

23868007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5003652-A-G

23868013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5003646-T-C

23868014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5003642-T-C

23875738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5000723-T-C

23875755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5000707-T-C

http://identifiers.org/hco/2/GRCh38#23880695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4994964-C-A

http://identifiers.org/hco/2/GRCh38#23880882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4994785-A-C

23880882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4994785-A-G

23880882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4994785-A-T

http://identifiers.org/hco/2/GRCh38#23880947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4994708-C-A

23880947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4994708-C-T

23884275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4993692-A-G

23885243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4992770-T-C

23885260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4992710-A-G

http://identifiers.org/hco/2/GRCh38#23885701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4992098-A-C

23885701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4992098-A-G

23885770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4992029-G-A

23885770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 4992029-G-T

23885874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4991916-A-G

http://identifiers.org/hco/2/GRCh38#23885883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4991907-A-C

23885883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4991907-A-G

http://identifiers.org/hco/2/GRCh38#23885939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4991854-C-A

23885939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4991854-C-T

23887874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4990201-T-G

23887940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4990135-T-C

23888042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4990040-A-G

23888236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4989823-T-C

23888426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4989627-A-G

23888526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4989551-G-C

23888526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4989551-G-T

http://identifiers.org/hco/2/GRCh38#23888590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4989499-A-C

http://identifiers.org/hco/2/GRCh38#23888761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4989331-A-C

23895665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4987687-T-C

23895932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4987423-T-C

http://identifiers.org/hco/2/GRCh38#23896441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4986905-A-C

http://identifiers.org/hco/2/GRCh38#23897589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4986053-C-A

23897661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4986005-T-C

23897675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4985991-G-A

23901245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982791-T-C

23902033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981530-C-T

23902244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981348-G-A

23902279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981313-A-G

23902731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980876-T-G

23902780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980836-T-C

http://identifiers.org/hco/2/GRCh38#23904888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4980483-A-C

23904889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980482-A-G

23904984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980390-A-G

23905022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980355-T-C

23914461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977594-G-A

http://identifiers.org/hco/2/GRCh38#23914656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4977447-A-C

23914656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977447-A-T

23915019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977176-C-T

23915953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976332-A-G

23915986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976297-G-A

23916114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976167-G-A

23916114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976167-G-C

23916114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976167-G-T

23916613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4975038-C-T

23916628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4975023-A-G

23916856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974800-T-C

23920745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972749-A-G

23920796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972690-A-G

23920842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972643-C-T

23920923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972566-G-C

23922891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971801-C-G

23923032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971658-A-G

23923257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971268-G-C

23923320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971217-G-A

http://identifiers.org/hco/2/GRCh38#23923400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4971106-A-C

23923902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970396-G-A

23924276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970187-T-C

23924368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970094-T-C

23924604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4969850-G-A

23924604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4969850-G-C

http://identifiers.org/hco/2/GRCh38#23924655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4969802-A-C

23924683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4969656-A-G

23925361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968989-T-C

23925496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968875-G-A

23926054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968362-G-A

23926418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968008-A-G

http://identifiers.org/hco/2/GRCh38#23926499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4967972-C-A

23926499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4967972-C-T

http://identifiers.org/hco/2/GRCh38#23926534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4967938-C-A

23926534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4967938-C-G

23926534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4967938-C-T

http://identifiers.org/hco/2/GRCh38#23926712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4967765-C-A

23926712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4967765-C-T

http://identifiers.org/hco/2/GRCh38#23926912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4967571-C-A

23926912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4967571-C-T

23926936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4967547-A-G

23927105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4967378-G-C

23927105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4967378-G-T