12901625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11802008-C-T

12901643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11802026-G-A

12901689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11802076-G-A

12901689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11802076-G-C

12901689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11802076-G-T

http://identifiers.org/hco/16/GRCh38#12901970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11802350-C-A

12901970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11802350-C-T

12902314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11802694-T-G

http://identifiers.org/hco/16/GRCh38#12902760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11803122-A-C

12902760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11803122-A-G

12902760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11803122-A-T

12902913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11803260-G-A

12902913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11803260-G-T

http://identifiers.org/hco/16/GRCh38#12902920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11803268-A-C

12902920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11803268-A-G

12902920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11803268-A-T

12903051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11803371-G-A

12903051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11803371-G-T

12903234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11803549-C-T

12903404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11803681-C-T

12903706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11803964-T-A

12904185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11804447-T-A

12904203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11804470-G-A

12904203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11804470-G-C

12904314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11804577-C-T

12904389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11804625-G-C

12904477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11804713-C-G

12904513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11804765-C-G

12904814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805035-G-T

12904835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805057-A-G

http://identifiers.org/hco/16/GRCh38#12905175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11805280-A-C

12905220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805326-G-A

12905286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805397-C-G

12905345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805444-G-A

12905465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805557-T-C

12906038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805768-A-G

12906223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11805916-G-T

12906363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11806028-T-C

12906373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11806038-C-G

12906787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11806858-G-A

12907068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807129-C-T

12907182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807162-T-C

12907182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807162-T-G

http://identifiers.org/hco/16/GRCh38#12907247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11807214-C-A

http://identifiers.org/hco/16/GRCh38#12907549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11807406-A-C

12907659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807518-G-A

12907681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807540-T-C

12907791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807644-C-G

12907791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807644-C-T

12908038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807818-G-T

12908197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807970-T-C

12908200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11807973-G-A

http://identifiers.org/hco/16/GRCh38#12908343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808102-C-A

12908369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11808128-G-A

12908369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11808128-G-C

12908479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 11808237-G-A

12908479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11808237-G-T

12908507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808265-G-T

http://identifiers.org/hco/16/GRCh38#12908535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808293-C-A

12908535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808293-C-G

12908535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808293-C-T

12908597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808361-G-C

12908697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808459-T-C

http://identifiers.org/hco/16/GRCh38#12908713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808473-A-C

http://identifiers.org/hco/16/GRCh38#12908817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808575-A-C

12908817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808575-A-G

12908817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11808575-A-T

http://identifiers.org/hco/16/GRCh38#12908983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808757-C-A

http://identifiers.org/hco/16/GRCh38#12908989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808763-A-C

http://identifiers.org/hco/16/GRCh38#12909102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11808868-A-C

12909102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11808868-A-G

12909191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11808935-T-C

12909226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11808953-G-A

12909226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11808953-G-T

12909252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11808979-C-T

12909306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809034-A-G

12909370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809102-T-A

12909370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809102-T-C

12909393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809125-A-G

12909467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809439-G-A

12909493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809465-T-C

12909534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809506-A-T

12909790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11809780-T-A

12912510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11811829-G-A

12912510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11811829-G-T

12912736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11812049-C-T

12913769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11812872-G-A

12913822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11812927-C-T

http://identifiers.org/hco/16/GRCh38#12914701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11813388-C-A

12915052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813698-G-C

12915052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813698-G-T

12915108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813755-T-G

12915571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813879-C-G

12915571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813879-C-T

12915658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813954-G-C

12915699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11813993-A-G

12915824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814112-A-G

12916288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814555-A-G

12916293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814560-A-G

http://identifiers.org/hco/16/GRCh38#12916485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11814718-A-C

12916501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814732-T-A

http://identifiers.org/hco/16/GRCh38#12916561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11814793-C-A

12916561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814793-C-G

12916625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814858-G-A

12916625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814858-G-T

12916659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11814888-G-A

12916758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11814987-G-A

12916758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11814987-G-T

12916798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11815027-C-T

http://identifiers.org/hco/16/GRCh38#12916846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11815074-C-A

12916846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815074-C-T

12916893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815118-T-C

12916980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815176-G-A

12916980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815176-G-T

12917084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815269-A-G

12917145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815344-C-T

12917159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815358-G-A

12917216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815435-G-T

12917610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815774-A-G

12917698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11815854-A-G

http://identifiers.org/hco/16/GRCh38#12917882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11816031-C-A

12917882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816031-C-T

12917911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816059-G-T

12917940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816097-C-T

12917969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816126-C-T

http://identifiers.org/hco/16/GRCh38#12918155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11816323-C-A

12918370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816469-T-A

12918371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816470-G-A

http://identifiers.org/hco/16/GRCh38#12918399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11816498-A-C

12918424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816517-T-C

12918689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11816777-A-T

12918824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11817092-C-G

12918909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11817179-A-G

12919028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11817315-C-G

12919028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11817315-C-T

12919127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11817411-A-T

12919396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11817676-A-G

12920019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11818190-C-T

12920060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11818209-T-C

12920087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11818236-G-A

12920753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11818430-A-G

12921928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11819818-C-G

12922014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11819886-A-T

12924220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11822715-G-A

12924414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11822892-G-C

http://identifiers.org/hco/16/GRCh38#12924524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11822999-C-A

12924524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11822999-C-T

12924616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11823059-A-G

12925134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11823548-G-A

12925871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11824326-A-G

12926654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11824914-A-G

12926831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11825040-C-T

12926863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11825065-A-G

12926948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11825161-C-G

12927764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11825701-C-G

http://identifiers.org/hco/16/GRCh38#12927831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11825736-C-A

http://identifiers.org/hco/16/GRCh38#12928174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11826211-A-C

12928174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11826211-A-G

12928246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11826286-A-G

12928343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11826387-C-T

http://identifiers.org/hco/16/GRCh38#12928369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11826412-A-C

http://identifiers.org/hco/16/GRCh38#12932672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11827967-C-A

12932984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828324-G-C

12933070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828414-A-G

12933071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828415-C-G

12933071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828415-C-T

12933171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828515-A-G

12933171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828515-A-T

12933184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11828528-C-G

12933818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11829453-A-T

http://identifiers.org/hco/16/GRCh38#12934105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11829786-A-C

12934123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11829812-C-T

12934317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11830397-A-G

12934728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11830794-T-A

12934899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11830955-G-A

12934899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11830955-G-T

http://identifiers.org/hco/16/GRCh38#12935485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#11831951-A-C

12935793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11832041-A-G

http://identifiers.org/hco/16/GRCh38#12937015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11833066-C-A

12937015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833066-C-G

http://identifiers.org/hco/16/GRCh38#12937062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11833110-C-A

12937062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833110-C-T

12937094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833141-C-T

12937182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833225-C-G

12937192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833235-T-G

12937414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833406-A-G

12937800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833709-G-A

12938053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11833939-C-G

12938188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11834087-G-A

12938475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11834361-C-T

12938843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11834425-T-C

12938950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11834512-C-T

http://identifiers.org/hco/16/GRCh38#12938965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11834527-C-A

12939591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11835077-C-T

12939596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11835082-G-A

12939735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11835209-A-G

12939820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11835277-C-G

12941705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11835845-G-T

12941723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11835863-T-C

12942191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11836412-T-G

12942348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11836525-C-T

12942393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11836571-C-T

12942416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11836594-C-T

12942435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11836611-A-G

12942516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11836688-G-T

12942917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11837313-G-T

12942977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11837379-C-G

http://identifiers.org/hco/16/GRCh38#12942978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11837380-A-C

12942978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11837380-A-T

12944583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11839736-G-A

12944607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11839758-G-C

12944946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840064-G-T

12947303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840204-C-T

12947526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840429-G-C

12947532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840435-C-T

12947554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840457-T-A

12947617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840500-C-G

12947636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840518-C-T

12947868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840748-C-G

12947868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11840748-C-T

12948339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11841160-G-A

12948506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11841347-A-G

http://identifiers.org/hco/16/GRCh38#12948539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11841388-A-C

12948703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11841564-A-G

12948815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11841644-T-G

12948862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11841679-C-T

12949177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11842312-G-A

12949607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11842670-T-C

12951505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11844218-C-T

12951616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11844315-T-C

12951617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11844316-T-C

12951816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11844656-G-T

http://identifiers.org/hco/16/GRCh38#12951863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11844702-C-A

12951969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11844811-T-C

12958560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11848317-G-C

12958760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11848513-G-A

12958792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11848544-T-G

http://identifiers.org/hco/16/GRCh38#12958981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11849450-C-A

12959009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11849477-C-T

12959255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11849709-C-G

http://identifiers.org/hco/16/GRCh38#12959262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11849729-C-A

12959288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11849755-G-A

12959288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11849755-G-T

12959289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11849756-G-A

12959542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11849912-G-C

12959693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11850058-G-A

12959765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11850110-C-T

12959795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11850136-T-G

12961902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11852783-C-T

12961956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11852827-G-C

12961960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11852830-C-G

12962066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11852938-A-G

12962073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11852945-C-T

http://identifiers.org/hco/16/GRCh38#12962108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11852980-C-A

12962119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11852991-G-A

http://identifiers.org/hco/16/GRCh38#12962262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11853129-C-A

12962262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853129-C-G

12962728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853532-G-T

12962742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853546-T-A

12962742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853546-T-C

http://identifiers.org/hco/16/GRCh38#12963024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11853793-C-A

12963087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853857-G-A

12963101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853867-G-T

12963104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853870-T-A

12963158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853920-C-T

12963187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853947-G-A

12963226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853973-T-C

12963251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11853999-A-G

12963825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854469-G-A

12963886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854524-A-G

12963947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854584-G-A

12963947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854584-G-T

12964111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854726-T-C

12964333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854955-G-A

12964355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11854988-G-T

12964371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855004-C-T

12964462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855082-G-A

12964462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855082-G-T

12964482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855102-G-T

12964639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855212-T-C

12964739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855303-A-G

12964874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855414-A-G

12964874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855414-A-T

12965031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11855576-C-G

12971357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11858895-G-A

http://identifiers.org/hco/16/GRCh38#12971384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11858922-C-A

12971595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11859132-A-G

12971662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11859197-G-A

12971669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11859218-C-T

http://identifiers.org/hco/16/GRCh38#12972020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11859613-A-C

12972170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11859875-G-T

12972463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11860117-G-A

12972801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11860453-T-C

12973595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11860847-G-A

12973665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11860900-G-C

12973710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11860946-A-G

12974134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862197-G-A

12974300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862358-A-G

http://identifiers.org/hco/16/GRCh38#12974440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11862484-A-C

12974440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862484-A-G

12974867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862649-A-G

12974906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862686-A-G

12975060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862833-A-G

12975061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862834-C-G

12975061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11862834-C-T

http://identifiers.org/hco/16/GRCh38#12975672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11863227-A-C

12975691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11863246-T-A

12975691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11863246-T-G

12975717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11863270-A-G

12976042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11863570-T-C

http://identifiers.org/hco/16/GRCh38#12976800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11864495-C-A

http://identifiers.org/hco/16/GRCh38#12977180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11864850-A-C

12977255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11864913-C-T

12978279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865248-C-T

12978318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865282-T-C

12978373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865320-C-T

12978402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865349-G-A

http://identifiers.org/hco/16/GRCh38#12978443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11865394-A-C

12978488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865424-G-A

12978637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865571-G-A

http://identifiers.org/hco/16/GRCh38#12978821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11865770-A-C

http://identifiers.org/hco/16/GRCh38#12978963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11865891-C-A

12978963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11865891-C-G

http://identifiers.org/hco/16/GRCh38#12979063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11865969-C-A

12979180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11866074-C-T

12979548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11866409-T-G

12979675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11866529-T-C

12979877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11866724-C-G

12979877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11866724-C-T

12980019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11866892-T-C

12980250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11867483-A-G

12980297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11867538-T-G

12980616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11867975-G-T

12980630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11867986-T-C

12980648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868007-A-T

12980756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868089-T-C

12980757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868090-G-A

12980908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868230-T-G

12981075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868378-C-T

12981125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868445-A-G

12981152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868475-T-A

12981199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11868520-A-G

12981798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869136-C-T

12981846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869166-G-C

12981954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869262-C-G

12981989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869297-A-T

12982324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869579-G-T

12982325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869580-T-C

12982342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11869597-C-T

12982510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870019-C-G

12982510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870019-C-T

12982711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870192-T-G

12982747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870245-C-G

12982992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870647-C-T

12983069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870723-C-G

12983099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870753-T-G

12984336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11870933-T-G

12984478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11871075-C-T

http://identifiers.org/hco/16/GRCh38#12984646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11871241-C-A

12984670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11871264-G-A

12984670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11871264-G-C

12984708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11871301-C-G

12987929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11874444-A-G

http://identifiers.org/hco/16/GRCh38#12987964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11874480-C-A

12988056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11874545-G-C

http://identifiers.org/hco/16/GRCh38#12991052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11876987-C-A

http://identifiers.org/hco/16/GRCh38#12991383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11877326-C-A

12991846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11877764-T-C

12991882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11877800-A-T

12992613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11878244-C-G

12992776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11878314-G-C

12992795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11878333-G-T

12995457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11879357-A-G

12995650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11879551-A-T

12995728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11879622-T-C

12995763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11879671-C-T

12995911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11879809-A-G

12996085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11879986-G-A

12996139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880038-A-G

12996141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880040-C-T

12996313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880180-T-A

12996512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880395-T-C

12996630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880501-G-A

12996700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880577-T-C

12996773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11880650-A-G

12997232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11881111-T-C

12997395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11881265-T-C

12999210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11883932-A-G

12999246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11883958-G-T

http://identifiers.org/hco/16/GRCh38#12999253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11883965-C-A

12999253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11883965-C-T

12999444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11884135-A-T

12999496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11884183-C-G

12999921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11884822-C-T

http://identifiers.org/hco/16/GRCh38#12999942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11884840-C-A

13000001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11884886-C-T

13000108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11885100-C-G

13000219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11885248-G-C

13000537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11885561-A-G

13000550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11885574-G-A

13001223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886117-C-T

13001286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886197-G-A

13001612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886499-A-G

13001687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886568-C-G

13001706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886587-A-G

13001787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886667-A-G

13001845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886723-A-G

13001867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11886900-A-T

13002168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11887174-C-T

13002219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11887217-T-C

13002226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11887224-T-C

13002240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11887238-G-T

13003120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11888598-G-C

13003133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11888611-T-C

13003288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11888767-A-G

13003288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11888767-A-T

13003354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11888817-T-A

13005132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11890542-G-C

13005219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11890629-C-T

13005312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11890723-A-G

http://identifiers.org/hco/16/GRCh38#13006023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11891412-C-A

13006097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891493-G-A

13006119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891514-G-A

13006163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891552-T-C

13006164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891553-T-C

13006164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891553-T-G

13006190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891581-T-C

13006211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11891603-C-T

http://identifiers.org/hco/16/GRCh38#13006341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11891735-A-C

13006762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11892271-C-G

13006821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11892353-T-C

13007083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11892618-C-G

13007083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11892618-C-T

http://identifiers.org/hco/16/GRCh38#13007137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11892673-C-A

13012278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11893908-G-C

13012487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894098-G-A

13012562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894160-G-A

http://identifiers.org/hco/16/GRCh38#13012598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11894192-C-A

13012903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894481-C-G

13012983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894563-C-T

13013346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894911-G-A

13013346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894911-G-T

13013360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894928-T-C

13013373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894954-G-T

http://identifiers.org/hco/16/GRCh38#13013390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11894971-C-A

13013390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894971-C-T

13013414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11894993-C-T

13013459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11895038-G-C

13013496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11895080-C-T

13021150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11898984-G-A

13021171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899008-T-C

13021218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899057-T-A

13021262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899098-T-C

13021341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899206-G-C

http://identifiers.org/hco/16/GRCh38#13021449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11899404-A-C

13021449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899404-A-G

13021464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899419-G-A

13021528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899482-G-A

13021531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899485-G-C

13021532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899486-C-T

13021840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899567-G-A

13021857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899578-G-C

13021909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899634-C-G

13021914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899639-T-G

13022000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899695-C-G

13022063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899754-G-A

13022087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899778-T-G

13022114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899804-G-C

13022289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11899931-C-T

13024081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11900560-A-G

13024147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11900607-G-A

13024221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11900677-T-C

13024331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11900786-C-T

13029871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11906516-C-G

http://identifiers.org/hco/16/GRCh38#13030036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11906673-C-A

13030224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11906857-T-G

13030344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11906964-C-G

13030509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11907095-G-A

13030509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11907095-G-C

13030869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11907830-A-G

13030954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11907916-G-A

13030954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11907916-G-T

13031134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908064-G-T

13031286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908208-A-T

13031433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908359-T-A

13031433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908359-T-G

13031435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908361-G-T

13031443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908369-G-A

13031443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908369-G-T

13031553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908468-A-G

13031941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908843-C-T

13031955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11908849-A-T

13032512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11909155-A-G

13032581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11909224-T-A

13032771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11909384-T-A

13032977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11909829-A-G

13033031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11909883-C-G

13033031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11909883-C-T

13033235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11910091-T-C

13034440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11910877-A-G

13034455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11910892-A-G

http://identifiers.org/hco/16/GRCh38#13034574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11911038-C-A

13034574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911038-C-G

13034574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911038-C-T

13034906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911369-G-A

13034935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911393-C-G

13035315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911640-C-G

http://identifiers.org/hco/16/GRCh38#13035360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11911677-C-A

13035360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911677-C-T

13035800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11911830-A-G

13036069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912093-A-G

13036254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912269-G-C

13036271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912286-T-C

13036279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912294-T-C

13036281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912296-T-C

13036326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912338-A-T

13036474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912484-G-A

13036477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912487-G-A

13036591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11912579-G-A

http://identifiers.org/hco/16/GRCh38#13037090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11913066-A-C

http://identifiers.org/hco/16/GRCh38#13037105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11913081-C-A

13037105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913081-C-G

13037107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913083-C-G

13037127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913103-C-G

13037160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913149-T-G

13037180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913168-C-T

13037386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913390-T-C

13037481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11913485-G-A

13039442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11914604-A-T

13039459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11914621-C-G

13039528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11914678-A-G

13039528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11914678-A-T

13039539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11914689-G-A

13039824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11914969-C-T

http://identifiers.org/hco/16/GRCh38#13039836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11914981-C-A

13039914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11915054-C-G

13039914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11915054-C-T

13040126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11915190-A-G

13040127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11915191-G-A

13040241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11915318-C-G

http://identifiers.org/hco/16/GRCh38#13046826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11916205-C-A

13046873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916242-T-C

http://identifiers.org/hco/16/GRCh38#13046917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11916281-C-A

13047044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916349-A-G

13047082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916384-C-G

13047195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916504-C-G

13047260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916564-A-G

13047264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916568-G-A

13047541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916807-C-T

http://identifiers.org/hco/16/GRCh38#13047626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11916893-A-C

13047697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11916964-G-A

13047749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917016-C-T

13047838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917105-C-G

13047838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917105-C-T

13047839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917106-G-A

13047839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917106-G-T

13047920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917175-G-A

13047920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11917175-G-C

13048333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11918096-G-A

13048769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11918662-A-G

13048790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11918685-C-T

13049135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11919893-T-C

13049323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11920261-T-C

13049394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11920332-A-G

13049581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11920504-G-A

13049695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11920613-A-G

13049704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11920622-C-T

http://identifiers.org/hco/16/GRCh38#13050689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11922115-C-A

13050728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922156-A-T

13050799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922224-T-C

13050851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922273-G-A

13050851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922273-G-T

13050900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922322-C-G

13051524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922551-C-T

13051605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922634-A-G

13052075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922778-A-G

13052161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922869-A-G

13052179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922881-G-A

http://identifiers.org/hco/16/GRCh38#13052186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11922888-A-C

13052210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11922912-G-A

13052396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11923092-C-T

13052400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11923096-G-A

13052481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11923164-C-G

13052587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11923261-C-G

13052587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11923261-C-T

13054614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11924222-C-T

13054849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11924420-C-T

http://identifiers.org/hco/16/GRCh38#13054977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11924548-C-A

13055640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11925871-G-T

13055828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11926419-T-A

http://identifiers.org/hco/16/GRCh38#13055999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11926669-A-C

13056034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11926733-A-T

13056112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11926799-G-C

13056230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11926914-A-G

13061265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11929132-T-A

13061384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11929287-C-G

13061388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11929291-T-C

13061890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11929848-G-A

http://identifiers.org/hco/16/GRCh38#13062175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11930251-A-C

13062350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930416-T-C

http://identifiers.org/hco/16/GRCh38#13062433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11930492-C-A

13062433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930492-C-T

13062434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930493-A-G

13062448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930507-C-T

http://identifiers.org/hco/16/GRCh38#13062533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11930577-C-A

13062533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930577-C-G

13062561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930597-G-C

13062586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930622-G-T

13062603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930639-G-A

13063811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930902-C-T

13063819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930910-T-G

13063886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11930961-A-G

http://identifiers.org/hco/16/GRCh38#13067044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11931174-A-C

13067214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931212-C-T

13067243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931239-A-T

13067458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931408-T-A

13067564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931528-C-T

13067621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931545-G-C

13067718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931602-T-C

13067790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931646-C-T

http://identifiers.org/hco/16/GRCh38#13067806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11931662-C-A

13067855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931706-A-G

13067929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931777-C-T

13067967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931808-T-A

13068134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11931966-T-C

13068418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932322-G-A

13068574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932463-G-A

http://identifiers.org/hco/16/GRCh38#13069628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11932636-C-A

13069628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932636-C-G

13069630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932638-G-A

13069673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932678-G-A

13069804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932812-G-A

13069804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11932812-G-T

13070052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11933043-T-A

13070249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11933193-C-G

13070298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11933240-C-T

13070536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11933485-G-T

13070772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11933713-C-T

13072255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11935242-C-T

13072468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11935390-G-T

http://identifiers.org/hco/16/GRCh38#13072907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11935839-C-A

13073225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936204-T-A

13073225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936204-T-C

http://identifiers.org/hco/16/GRCh38#13073247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11936226-A-C

13073452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936393-C-G

13073452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936393-C-T

13073559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936470-T-A

13073559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936470-T-G

13073787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936601-C-T

13073798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936612-C-G

13073798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11936612-C-T

http://identifiers.org/hco/16/GRCh38#13074329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11937228-C-A

13074353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11937255-C-G

13075173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11937737-C-G

13075225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11937789-C-T

13078032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11940489-C-T

13079176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11942860-A-G

13079333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11942956-G-A

13079378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943005-C-G

13079501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943113-T-A

13079508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943120-C-T

13079850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943491-G-C

13079905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943562-T-C

13079905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943562-T-G

13079952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943605-C-G

13080037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943688-T-A

13080043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943694-C-T

13080096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11943740-G-A

13080549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11944188-C-G

13080596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11944240-G-A

13080605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11944272-G-C

13080670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11944515-T-C

13080929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11944780-C-T

13080997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11944852-A-G

13081209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11945058-T-C

13082468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11946101-T-C

13082498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11946127-A-G

http://identifiers.org/hco/16/GRCh38#13082509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11946138-C-A

13082535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11946164-G-A

13082535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11946164-G-T

13082635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11946251-T-C

13082699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11946311-T-A

http://identifiers.org/hco/16/GRCh38#13082931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11946578-C-A

13083607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11947597-A-G

13083819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11947806-C-T

13083905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11947893-G-A

13083913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11947901-C-T

13083920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11947908-G-A

13083972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11947959-G-A

13084168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11948149-C-G

13093448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11949845-C-G

http://identifiers.org/hco/16/GRCh38#13093592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11949985-C-A

13093629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950023-C-T

13093847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950239-A-G

13093954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950347-G-C

13093994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950387-T-C

13094138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950526-A-T

13094197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950586-C-T

13094255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11950639-A-G

http://identifiers.org/hco/16/GRCh38#13094846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11951211-C-A

13094868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11951233-G-C

13095008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11951360-C-G

13095817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11951927-A-G

13095931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952032-C-G

13095931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952032-C-T

13096146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952214-A-G

13096151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952219-C-G

13096152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952220-A-G

13096220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952283-T-G

13096349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952336-G-A

http://identifiers.org/hco/16/GRCh38#13096623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11952581-C-A

13096832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952766-A-T

13096945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11952952-T-C

13097031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953005-A-G

13097818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953426-T-C

13097855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953463-C-T

13097902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953508-G-A

13097902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953508-G-T

13098014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953624-T-G

13098065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953674-C-G

13098257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953862-T-C

13098337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11953957-A-G

13098397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954011-T-C

13098409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954023-G-A

13098493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954110-C-T

13098545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954375-C-G

13098545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954375-C-T

13098557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954387-C-G

13098700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954530-G-C

13098705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11954535-C-T

13099853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11957990-C-T

13099968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11958093-A-G

13100208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11958332-G-A

13100297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11958416-T-C

13100681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11959494-T-C

13100775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11959589-T-G

13101331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960090-A-T

13101374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960133-G-A

13101374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960133-G-T

13101408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960163-A-G

http://identifiers.org/hco/16/GRCh38#13101417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11960172-C-A

13101443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960195-T-C

13101515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960271-C-T

13101621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960746-C-T

http://identifiers.org/hco/16/GRCh38#13101667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11960792-A-C

13101697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960823-C-T

13101711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11960837-C-G

13101896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961019-G-A

13101909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961032-A-G

13102401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961468-C-T

13102469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961514-G-A

13102566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961601-C-G

13102621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961656-A-G

13102856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11961854-C-G

13104194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963310-T-C

13104418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963530-A-G

13104456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963569-A-G

13104567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963682-A-G

13104621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963730-C-T

http://identifiers.org/hco/16/GRCh38#13104733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11963836-C-A

13104733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963836-C-T

http://identifiers.org/hco/16/GRCh38#13104801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11963930-C-A

13104801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11963930-C-G

13104901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11964027-A-G

http://identifiers.org/hco/16/GRCh38#13105069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11964196-C-A

13105246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11964366-G-A

13105458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11964571-T-G

13105748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11964866-C-T

13105755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11964872-A-T

13105759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11964876-C-T

http://identifiers.org/hco/16/GRCh38#13105800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11964901-A-C

13106061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965151-G-A

13106267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965354-G-A

13106465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965541-G-A

13106511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965587-C-T

13106615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965669-G-A

13106628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965686-G-C

13106644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965702-G-A

13106692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11965750-T-G

13107730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11968304-A-T

13107811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11968230-A-G

13107886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11968180-T-G

13109924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11969133-T-C

13109948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11969157-T-C

13109971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11969180-G-C

13110138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11969480-C-T

http://identifiers.org/hco/16/GRCh38#13110217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#11969555-C-A

13110346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11969668-G-T

13110511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11969844-G-A

13110749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11970071-G-A

13110749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11970071-G-T

13111449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11970359-T-C

13111824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11970651-G-A

13111824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11970651-G-T

13111904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11970717-C-G

13111948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11970761-A-G

13112026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11970845-T-G

13112687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11971987-G-A

13112873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11972158-T-G

13112907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11972192-G-A

13113282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11972250-T-G

13113659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11972592-A-G

13114006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11972927-C-T

13114727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11973303-T-A

http://identifiers.org/hco/16/GRCh38#13114928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11973565-A-C

13114970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11973607-A-G

13114988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11973625-A-G

13115029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11973673-T-C

13115868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974267-A-G

13115875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974274-G-C

13115934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974345-C-G

13116056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974462-T-C

13116084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974492-G-A

13116207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974609-C-G

13116254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11974656-G-C

13119555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11976548-A-G

13119577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11976597-G-A

13119580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11976600-A-G

13120160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11977156-G-A

13120160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11977156-G-C

13120217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11977213-G-T

13120264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11977266-G-A

http://identifiers.org/hco/16/GRCh38#13120361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11977356-A-C

13121598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978094-A-G

13121774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978270-T-C

13122081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978543-G-T

13122088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978550-T-C

http://identifiers.org/hco/16/GRCh38#13122329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11978781-C-A

13122396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978848-C-T

13122424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978885-A-G

13122508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11978966-G-A

http://identifiers.org/hco/16/GRCh38#13122663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11979114-C-A

13122709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11979160-C-G

13123168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11979279-A-G

13123309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11979387-A-G

http://identifiers.org/hco/16/GRCh38#13123905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11980001-C-A

13123995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11980086-T-G

13124078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11980177-A-G

13124438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11980536-G-C

13124516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11980623-G-T

13124537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11980644-G-T

13125760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11981286-C-G

13125760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11981286-C-T

13126355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11981860-A-G

13126446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11981940-G-A

13127590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11982061-C-G

13127605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11982081-G-C

13128274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11982729-C-T

13129686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11985826-G-C

13129686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11985826-G-T

13130468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11987152-A-G

13130561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11987246-G-A

http://identifiers.org/hco/16/GRCh38#13131778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11987844-C-A

13132007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988117-T-A

13132007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988117-T-C

13132237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988308-A-G

13132245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988316-T-C

13132394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988453-G-A

http://identifiers.org/hco/16/GRCh38#13132412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11988469-C-A

13132412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988469-C-T

13132590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11988640-C-G

13133075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989040-T-C

13133077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989042-G-T

13133128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989093-A-G

13133144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989107-G-T

13133243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989203-G-A

13133278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989235-C-G

13133661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989547-C-T

13133702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989587-A-G

13133841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989726-G-A

13133988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11989885-A-G

13134323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11990203-A-G

13134409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11990289-A-T

13134496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11990374-T-C

13134689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11990638-C-T

13134971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11990869-C-T

13134982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11990880-C-T

13135211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11991025-G-A

13135320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11991123-C-T

13135321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11991124-C-T

13135387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11991184-A-G

13135387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11991184-A-T

13136193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11992004-A-G

13136256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11992076-T-C

13136811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11992811-C-G

13136853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11992855-T-A

13136888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11992890-C-T

13137078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11993070-G-C

13137323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11993313-G-A

13139877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11996403-C-T

13139996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11996520-G-A

13140033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11996551-T-C

13140493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11996569-G-A

13140528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11996604-A-G

13140617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11996669-G-A

http://identifiers.org/hco/16/GRCh38#13141051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11997083-C-A

13141051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997083-C-G

13141217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997240-A-G

13141256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997275-G-A

13141842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997442-G-C

13142057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997633-T-G

13142084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997658-C-T

http://identifiers.org/hco/16/GRCh38#13142189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#11997756-C-A

13142189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997756-C-T

13142313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997879-C-T

13142314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997880-G-A

13142352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997918-A-G

13142355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11997921-A-G

13142573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12004139-C-G

http://identifiers.org/hco/16/GRCh38#13142586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12004152-C-A

13142746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12004276-G-A

13143367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12004510-G-A

13143578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12004740-T-C

13143615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12004777-T-C

13143916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005053-G-C

13143929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005066-C-T

13144009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005150-G-A

13144084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005222-A-G

13144244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005294-C-G

13144526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005379-T-C

http://identifiers.org/hco/16/GRCh38#13144531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12005384-A-C

13144645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005482-A-G

13144732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005568-G-T

13144809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005644-G-A

13144914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005751-G-C

13145059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12005899-C-T

13145225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006068-G-A

13145711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006203-A-G

13146621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006777-C-T

13146649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006805-C-T

http://identifiers.org/hco/16/GRCh38#13146725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12006876-C-A

13146725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006876-C-T

13146773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006923-A-T

13146814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12006995-G-T

13146862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12007077-T-C

13147004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12007185-G-A

13147112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12007291-G-A

13147208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12007787-T-A

13147344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12007947-C-T

13147421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12008021-A-T

13147794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12014253-C-T

http://identifiers.org/hco/16/GRCh38#13148334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12014984-C-A

13148334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12014984-C-G

13148493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015151-C-T

13148504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015162-T-C

13148531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015189-C-G

13148531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015189-C-T

13148617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015261-A-G

13148637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015281-T-C

13148661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015305-A-G

13148873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015537-A-G

13149040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015734-G-A

13149046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015747-G-C

13149093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015794-T-C

13149148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015846-C-G

13149148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12015846-C-T

13150004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12016734-T-A

http://identifiers.org/hco/16/GRCh38#13150005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12016735-C-A

13150005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12016735-C-T

http://identifiers.org/hco/16/GRCh38#13150094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12016798-C-A

13150265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12016953-T-A

13150552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12017300-C-T

13150650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12017392-T-C

13150925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12017602-C-T

13151026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12017713-G-A

13151059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12017747-G-A

13152187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12018481-T-A

13152235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12018528-C-T

13152708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12018948-G-A

13152743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12018982-C-T

13152800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019034-C-T

13152813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019047-T-C

13152924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019160-C-T

13153174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019599-C-G

13153174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019599-C-T

13153211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019636-C-T

13153292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019706-C-T

13153572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12019954-C-T

13153649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12020030-C-G

13153947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12020330-G-A

13154053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12020430-G-A

http://identifiers.org/hco/16/GRCh38#13154128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12020504-C-A

13155721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12021740-C-T

13155759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12021818-T-C

13155824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12021881-G-T

13155950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12022020-G-A

13156308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12022349-G-A

13157785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12022837-G-A

13158227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12023386-A-G

13158478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12023627-G-A

13158648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12023778-T-G

13159386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12025662-T-C

13159462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12025711-G-A

13159546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12025785-C-G

13159623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12025840-C-G

13159643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12025860-T-C

13159801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026008-A-G

13159905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026101-G-T

http://identifiers.org/hco/16/GRCh38#13160149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12026255-A-C

13160199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026296-C-T

http://identifiers.org/hco/16/GRCh38#13160235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12026332-A-C

13160235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026332-A-G

13160249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026344-G-A

13160392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026482-T-C

13160575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026623-C-T

13160733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026770-T-G

13160922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026924-T-A

13160956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026959-A-T

13160978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026980-A-G

13160979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026981-G-A

13160979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12026981-G-T

13161186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027166-G-C

13161453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027408-C-G

13161705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027510-A-G

13161802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027607-G-A

13161821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027629-G-A

13161960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027668-T-C

13162257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027883-G-A

13162308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12027932-C-T

13162473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12028096-A-G

13162557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12028178-A-G

http://identifiers.org/hco/16/GRCh38#13162712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12028317-A-C

13162785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12028390-G-A

13165546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12033904-C-T

13165585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12033940-C-T

13165629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12033988-T-C

13165727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034080-C-T

13165741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034094-G-C

13165883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034234-A-G

13165922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034273-C-T

13165965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034316-T-C

13165965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034316-T-G

13168355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12034884-G-A

13168412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12034939-C-G

13168412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12034939-C-T

13168742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035220-G-A

http://identifiers.org/hco/16/GRCh38#13168921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12035361-A-C

13168921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035361-A-G

13168944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035378-G-A

13169067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035500-G-C

13169124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035563-C-T

13169448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035885-C-T

13169549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12035985-T-C

13169803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036223-C-T

13169841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036261-C-T

13169886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036303-G-T

13171401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036484-G-A

http://identifiers.org/hco/16/GRCh38#13171515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12036543-C-A

13171515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036543-C-G

13171584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036605-A-T

13171629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036651-C-T

13171896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036896-T-C

13171913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12036913-A-G

http://identifiers.org/hco/16/GRCh38#13172044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12037070-C-A

http://identifiers.org/hco/16/GRCh38#13172063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12037108-C-A

13172063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12037108-C-T

http://identifiers.org/hco/16/GRCh38#13172251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12037285-C-A

13172286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12037315-C-T

13172398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12037389-C-T

13172451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12037446-T-A

13172451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12037446-T-C

13172604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12037587-A-G

13173022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038004-C-T

13173150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038128-T-C

13173401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038654-C-G

13173415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038668-C-G

13173434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038687-G-A

13173434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038687-G-C

13173563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038799-C-T

13173574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038810-T-C

http://identifiers.org/hco/16/GRCh38#13173601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12038837-C-A

13173688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12038941-C-T

13173773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12039014-C-T

13173826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12039065-G-A

13176714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12041945-G-A

13177212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12042438-C-G

13177391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12042649-A-G

13177429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12042680-T-C

13178062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12042957-C-T

13178385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043251-G-A

13178431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043297-T-C

13178497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043363-C-G

13178755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043598-G-A

13178755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043598-G-C

13179426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043904-A-G

13179446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12043924-A-G

13179542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044019-C-G

13179542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044019-C-T

http://identifiers.org/hco/16/GRCh38#13179593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12044069-A-C

13179794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044265-T-G

13179806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044277-G-A

13180037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044538-C-T

13180062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044562-G-A

13180126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12044621-C-T

13181138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12045155-T-A

13181448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12045392-G-A

http://identifiers.org/hco/16/GRCh38#13188133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12047536-C-A

13188318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12047736-T-C

13188318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12047736-T-G

13188401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12047809-T-C

13188410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12047818-G-A

13188418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12047826-C-T

13188439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12047847-T-C

13189996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12048836-T-C

13189997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12048837-G-A

13190003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12048843-A-G

13190004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12048844-G-A

13190078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12048918-A-G

13190274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049199-C-T

13190311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049232-A-G

13190347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049259-G-C

13190436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049388-G-A

13190493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049443-C-T

13190522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049492-T-C

13190572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049577-G-A

13190581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049619-G-A

http://identifiers.org/hco/16/GRCh38#13190657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12049840-C-A

13190657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049840-C-T

http://identifiers.org/hco/16/GRCh38#13190722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12049914-C-A

13190722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12049914-C-G

13190984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050137-C-T

13191241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050427-C-T

13191262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050448-A-G

13191342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050536-C-G

13191375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050548-A-G

13191515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050681-T-C

13191605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050765-A-G

13191623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050782-G-A

13191651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050808-G-C

http://identifiers.org/hco/16/GRCh38#13191653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12050810-C-A

13191716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12050867-G-A

13192982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051205-G-A

13193268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051452-C-T

http://identifiers.org/hco/16/GRCh38#13193433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12051502-C-A

13193615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051643-T-G

13193707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051732-G-C

13193719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051744-G-A

13193727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051752-G-A

13193730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12051755-G-C

13193963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052270-A-G

http://identifiers.org/hco/16/GRCh38#13193971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12052276-C-A

13193971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052276-C-T

13194002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052305-A-G

13194368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052648-T-C

13194374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052654-G-C

13194423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052707-G-T

13194472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052754-C-T

13194481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12052763-G-A

http://identifiers.org/hco/16/GRCh38#13194700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12053001-C-A

13196522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12055980-T-A

13196605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056058-G-C

13196616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056069-T-C

13196821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056294-C-T

13197043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056593-G-C

13197058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056606-C-G

13197058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056606-C-T

http://identifiers.org/hco/16/GRCh38#13197131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12056736-A-C

13197145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056743-G-A

http://identifiers.org/hco/16/GRCh38#13197147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12056745-A-C

13197147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056745-A-G

13197157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056755-A-G

13197249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056831-C-T

13197277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056859-C-G

13197277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056859-C-T

13197317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12056897-C-G

http://identifiers.org/hco/16/GRCh38#13197623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12057192-A-C

http://identifiers.org/hco/16/GRCh38#13197626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12057195-C-A

13197634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12057203-T-C

13197668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12057240-A-G

13197766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12057321-G-T

13197804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12057355-T-C

13198516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12057594-T-C

http://identifiers.org/hco/16/GRCh38#13198529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12058754-C-A

13198529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12058754-C-T

13198576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12058801-C-G

13198603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12058822-A-G

13198877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059101-C-G

13199117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059337-G-T

13199126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059346-A-G

13199126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059346-A-T

13199137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059357-G-T

13199154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059374-T-C

13199274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059493-G-A

13199274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12059493-G-C

http://identifiers.org/hco/16/GRCh38#13203413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12062491-C-A

13203413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12062491-C-G

13203413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12062491-C-T

13203414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12062492-G-A

http://identifiers.org/hco/16/GRCh38#13203530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#12062608-C-A

13203530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 12062608-C-G

13203530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12062608-C-T

13203566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062645-G-A

13203615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062695-A-T

13203618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062698-T-C

http://identifiers.org/hco/16/GRCh38#13203653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12062727-C-A

13203653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062727-C-G

13203687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062755-G-A

13203687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062755-G-C

13203687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062755-G-T

13203698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062766-A-G

http://identifiers.org/hco/16/GRCh38#13203783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12062838-A-C

13203783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062838-A-G

13203786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062840-C-T

13203843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062898-T-C

http://identifiers.org/hco/16/GRCh38#13203972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12062961-A-C

13204022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12062983-T-C

13204144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063043-A-G

13204206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063087-G-A

13204214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063095-A-G

13204243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063124-T-C

13204303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063144-C-T

13204339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063179-A-G

http://identifiers.org/hco/16/GRCh38#13204680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12063543-C-A

13204680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063543-C-T

13204688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063551-G-T

13204695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063558-A-G

13204815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12063664-C-T

13204826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12063674-G-A

13204827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12063675-A-G

13204848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12063697-T-C

http://identifiers.org/hco/16/GRCh38#13204974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12063770-C-A

13204974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12063770-C-T

http://identifiers.org/hco/16/GRCh38#13205197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12064038-A-C

http://identifiers.org/hco/16/GRCh38#13205238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12064209-A-C

13205341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064339-G-A

13205893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064651-C-G

13205974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064685-C-T

13206049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064718-G-C

13206049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064718-G-T

13206102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064745-G-A

13206103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064746-G-T

13206221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064873-T-C

13206232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12064884-A-G

13206443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065059-C-G

13206501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065120-C-T

13206651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065249-A-G

13206660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065258-A-G

13206834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065442-T-C

13206857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065453-T-A

13206863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065459-G-A

13206863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065459-G-T

13206966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065557-T-C

13206980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065571-C-G

13207015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065606-A-G

13207345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12065827-A-G

13207559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066030-G-T

13207614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066078-C-T

13207794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066253-A-T

13208085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066541-C-G

13208101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066557-T-G

http://identifiers.org/hco/16/GRCh38#13208233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12066682-A-C

13208253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066709-C-T

13208277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066733-A-G

13208346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066800-C-G

http://identifiers.org/hco/16/GRCh38#13208598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12066919-A-C

13208626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066947-G-T

13208673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12066994-T-A

13208744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067071-C-T

http://identifiers.org/hco/16/GRCh38#13208840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12067166-C-A

13208882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067203-A-G

http://identifiers.org/hco/16/GRCh38#13208940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12067254-C-A

13209038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067356-G-T

13209206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067503-C-T

13209219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067520-C-T

13209563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067745-G-T

13209674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067855-C-G

13209674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067855-C-T

13209748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12067911-T-C

13210289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068123-T-A

13210388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068223-T-C

13210399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068234-T-A

13210413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068247-C-T

13210675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068495-A-T

13210871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068673-G-A

13210908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068705-T-C

13210938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068735-C-T

13210939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068736-C-G

13210939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068736-C-T

13211329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068867-T-A

13211329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068867-T-G

13211368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068906-G-A

13211436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068969-C-G

13211509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068998-G-A

13211509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12068998-G-T

http://identifiers.org/hco/16/GRCh38#13211560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12069064-C-A

13211560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069064-C-T

13211582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069090-C-T

13211623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069131-G-A

http://identifiers.org/hco/16/GRCh38#13211873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12069365-C-A

13211873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069365-C-T

13211920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069413-G-A

http://identifiers.org/hco/16/GRCh38#13211935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12069428-C-A

13211935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069428-C-T

13211993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069474-T-G

http://identifiers.org/hco/16/GRCh38#13212031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12069512-C-A

13212031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069512-C-T

13212297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12069785-T-C

13212731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070188-C-T

13212765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070211-A-T

13212805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070246-A-T

13212827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070268-G-A

13212867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070311-C-T

13212940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070380-A-G

http://identifiers.org/hco/16/GRCh38#13213001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12070430-C-A

13213420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070816-T-A

13213448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070844-G-A

13213448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070844-G-T

13213491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070918-G-A

http://identifiers.org/hco/16/GRCh38#13213492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12070919-C-A

13213513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070940-G-A

13213513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12070940-G-C

13213733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12071161-T-C

13213816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12071237-G-C

13213877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12071302-G-A

13213912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12071336-T-C

13214030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12071449-G-C

13215061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12071812-G-C

13215256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12072071-A-G

http://identifiers.org/hco/16/GRCh38#13215382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12072254-C-A

13215718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12072583-G-A

13215747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12072618-C-T

http://identifiers.org/hco/16/GRCh38#13215798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12072664-A-C

13215902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12072737-A-G

13216395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12073033-T-C

13216723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12073369-C-T

http://identifiers.org/hco/16/GRCh38#13216753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12073399-C-A

13216916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12074074-G-A

13216916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12074074-G-T

13216918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12074076-C-T

http://identifiers.org/hco/16/GRCh38#13217424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12074198-C-A

13217441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074215-C-G

13217441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074215-C-T

13217569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074332-A-G

13217588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074351-G-A

13217599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074362-A-G

13217599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074362-A-T

13217618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074416-G-T

13218185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074620-C-G

13218185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12074620-C-T

13218851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12075609-G-A

13218851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12075609-G-C

13219124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12075879-G-A

13219140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12075895-C-G

13219140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12075895-C-T

13220195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12076344-G-A

http://identifiers.org/hco/16/GRCh38#13220315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12076424-C-A

13220635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12076774-A-G

13220684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12076816-C-T

13220702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12076841-C-T

13221094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077153-A-G

13221317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077376-T-C

13221365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077429-G-A

13221365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077429-G-T

13221382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077447-C-G

13221382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077447-C-T

13221559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077613-C-T

13221571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12077625-G-A

13224387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12078848-T-C

13224452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12078913-G-A

13224525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12078989-C-G

http://identifiers.org/hco/16/GRCh38#13224780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12079202-A-C

13224872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079272-C-T

http://identifiers.org/hco/16/GRCh38#13224920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12079318-A-C

13224946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079345-A-T

http://identifiers.org/hco/16/GRCh38#13224972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12079368-C-A

13225055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079463-G-A

13225110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079511-C-T

13225173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079603-C-G

13225173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079603-C-T

13225310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079715-G-T

13225337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079742-A-G

http://identifiers.org/hco/16/GRCh38#13225372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12079776-C-A

13225372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079776-C-T

13225449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079851-G-C

13225450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079852-A-G

13225465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12079867-T-C

13225489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080312-G-A

13225490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080313-A-G

13225563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080386-G-C

13225674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080498-G-A

13225709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080532-A-G

13225759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080578-C-T

13225761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080580-C-T

13225831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080650-A-T

13225964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080787-T-A

13226015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080839-G-A

13226054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080878-G-T

13226055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12080879-G-A

13226347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081139-C-T

13226507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081300-G-A

13226509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081302-T-C

13226568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081361-G-T

13226579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081372-C-T

13226680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081460-G-C

13226720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081496-G-A

13226720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081496-G-T

13226747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081519-C-T

13226784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081556-T-G

13226845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081614-C-T

13226885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081643-T-C

13227798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081848-A-G

13227917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081950-T-C

13227936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12081966-A-G

13227993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12082023-A-G

13228041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12082066-G-A

13228041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12082066-G-T

13228662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12082561-G-C

13232192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12083152-G-C

13232246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12083205-G-A

13234140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12084171-A-G

13234207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12084231-C-T

13234826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12085091-T-C

13234907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12085169-G-T

http://identifiers.org/hco/16/GRCh38#13234978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12085235-C-A

13234978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12085235-C-G

13235087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12085345-C-T

13235205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12085463-A-G

13235341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12085599-C-T

http://identifiers.org/hco/16/GRCh38#13235364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12085622-A-C

http://identifiers.org/hco/16/GRCh38#13235519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12085794-C-A

13235519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085794-C-G

13235519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085794-C-T

13235616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085888-G-A

13235616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085888-G-C

13235616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085888-G-T

13235671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085928-C-T

13235718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12085953-G-A

http://identifiers.org/hco/16/GRCh38#13235736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12085970-C-A

13235890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086093-G-A

13236201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086353-G-C

13236201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086353-G-T

13236203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086355-G-A

http://identifiers.org/hco/16/GRCh38#13236392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12086495-C-A

13236462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086562-C-T

13236591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086693-T-G

13236866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086883-T-C

13236900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12086917-G-C

13237051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087063-C-T

13237181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087173-T-C

13237224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087208-G-A

13237261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087241-A-G

http://identifiers.org/hco/16/GRCh38#13237262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12087242-C-A

13237262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087242-C-G

http://identifiers.org/hco/16/GRCh38#13237295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12087273-C-A

13237295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087273-C-T

13237307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087285-A-G

13237365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087325-A-T

13237392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087333-G-A

13237564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087390-G-T

13237636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087422-G-A

13237636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087422-G-T

13237639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087425-G-A

13237639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087425-G-C

13237737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087435-C-G

13237737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087435-C-T

13237812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087459-T-A

13237817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087464-T-G

13237852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087497-G-A

13237860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087505-G-T

13237964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087606-C-T

13238295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087863-G-A

13238383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087946-G-A

13238383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087946-G-T

13238416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12087977-T-C

13238569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088111-A-G

13238679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088196-C-T

13239994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088374-G-A

13239994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088374-G-T

http://identifiers.org/hco/16/GRCh38#13240064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12088410-C-A

13240064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088410-C-T

13240090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088436-G-A

http://identifiers.org/hco/16/GRCh38#13240115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12088458-C-A

13240115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088458-C-T

13240229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12088586-C-T

13240455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12088804-A-G

http://identifiers.org/hco/16/GRCh38#13240511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#12088852-A-C

13240511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12088852-A-G

13240595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37231
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12088933-T-C