66964213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10039035-G-T

66964262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10039084-G-A

66964262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 10039084-G-T

66964349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10039171-A-G

66967386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10042264-C-G

66967559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10042456-G-A

66967571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10042468-C-T

http://identifiers.org/hco/8/GRCh38#66967655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10042739-A-C

66967749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10042837-G-A

66967963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043086-A-G

66968311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043431-C-T

66968319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043439-G-T

66968338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043459-G-T

http://identifiers.org/hco/8/GRCh38#66968358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10043479-C-A

66968373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043494-G-A

66968373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043494-G-T

66968501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043608-G-A

66968550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043657-T-A

66968550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10043657-T-C

66968712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10044418-T-C

66968724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10044430-C-G

66969131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10044802-T-G

66969434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045141-C-T

66969455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045166-C-T

66969587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045301-C-G

66969600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045314-C-T

66969854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045565-G-A

66970097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045880-A-G

66970281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10045973-C-T

66970513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046246-C-T

66970554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046287-T-C

66970628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046370-T-C

66970690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046437-T-C

http://identifiers.org/hco/8/GRCh38#66970717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10046452-C-A

66970717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046452-C-T

66970758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046489-C-T

http://identifiers.org/hco/8/GRCh38#66970790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10046521-C-A

66970790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046521-C-G

66970790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046521-C-T

http://identifiers.org/hco/8/GRCh38#66970827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10046672-C-A

66970833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046678-T-C

66970988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10046819-C-T

http://identifiers.org/hco/8/GRCh38#66971147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10046978-C-A

66971164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10046995-G-A

66971288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10047123-A-T

http://identifiers.org/hco/8/GRCh38#66980205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10047955-C-A

66980215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10047965-A-G

66981388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10048469-T-C

66981900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10048862-C-T

http://identifiers.org/hco/8/GRCh38#66981903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10048865-C-A

66981903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10048865-C-T

66982001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10048956-T-C

66982021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10049001-G-A

66982021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10049001-G-T

66982022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10049002-T-C

66982053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 10049045-G-A

66982053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 10049045-G-T

66982177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10049169-A-G

66983341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10051383-A-T

66987036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10052375-C-G

66987079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10052418-T-C

66988016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10054461-G-A

66988016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10054461-G-T

66988045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10054489-C-G

66988045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10054489-C-T

66988257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10055684-C-G

66988257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10055684-C-T

66988322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10055747-T-C

http://identifiers.org/hco/8/GRCh38#66988344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10055769-C-A

66988344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10055769-C-G

66988344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 10055769-C-T

66988526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10055943-A-G

66988526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10055943-A-T

66988573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10055990-T-C

66988587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10055997-T-C

http://identifiers.org/hco/8/GRCh38#66988651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10056055-C-A

66988651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10056055-C-T

66988767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10056143-C-T

66988817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10056194-G-T

66988843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10056220-A-G

66988871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10056249-G-A

66989147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10056966-A-G

66989417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10057248-C-G

66989417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10057248-C-T

66989992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10058521-T-C

http://identifiers.org/hco/8/GRCh38#66991011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10059459-A-C

66991257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10059755-A-G

66991294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10059830-G-A

66992140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061086-T-C

66992231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061163-T-G

66992536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061355-A-G

66992582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061383-T-A

66993077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061744-C-G

66993127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061763-C-T

66993213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061848-A-G

66993291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10061920-C-T

66993476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10062092-T-A

66993863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10062421-C-T

66994178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10062698-G-A

66994353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10062786-C-T

66994450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10062904-T-A

66994705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10063283-T-G

66994759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10063339-A-G

66995217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10063787-T-C

67010265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10064975-G-A

http://identifiers.org/hco/8/GRCh38#67010493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10065164-C-A

67010504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065175-G-A

67010504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065175-G-T

67010550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065219-G-A

67010550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065219-G-T

67010582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065243-G-T

67010586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065247-C-T

67010602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065263-A-G

http://identifiers.org/hco/8/GRCh38#67010610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10065271-C-A

67010610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065271-C-T

67010699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10065355-T-C

http://identifiers.org/hco/8/GRCh38#67010898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10065552-C-A

67010916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065572-T-A

67010916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065572-T-G

67010951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065597-G-A

67010951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065597-G-T

67010960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10065604-T-G

http://identifiers.org/hco/8/GRCh38#67010977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10065621-C-A

67011070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10066222-A-G

67012583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069284-T-C

67012594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069295-G-A

67012704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069391-A-G

67012752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069438-G-A

67012752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069438-G-T

67012765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069451-T-C

67012803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069484-G-A

67012803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069484-G-T

67012812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069493-A-T

67012831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069507-G-A

67012831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069507-G-T

67012864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069535-G-A

67012864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069535-G-T

67012866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069537-A-T

67012873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069544-C-T

67012880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069551-T-C

http://identifiers.org/hco/8/GRCh38#67012882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10069553-C-A

67012948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10069616-G-A

http://identifiers.org/hco/8/GRCh38#67013124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10069790-A-C

67013124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10069790-A-G

67014335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070106-A-T

http://identifiers.org/hco/8/GRCh38#67014340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10070111-A-C

67014357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070128-T-C

67014497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 10070267-G-C

67014497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 10070267-G-T

67014584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 10070354-G-T

67014613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070382-T-C

http://identifiers.org/hco/8/GRCh38#67014631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10070399-C-A

67014631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070399-C-G

67014631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070399-C-T

67014642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070410-A-G

67014802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070552-G-A

67014910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070657-C-T

67014914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070661-A-G

67014933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10070684-A-T

67015819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10071305-G-A

67015859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10071345-A-G

67016102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10072606-G-C

http://identifiers.org/hco/8/GRCh38#67017515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10073362-A-C

http://identifiers.org/hco/8/GRCh38#67017774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10073615-C-A

67017774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10073615-C-T

67017784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10073625-G-A

67017784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10073625-G-T

67017815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10073656-G-T

http://identifiers.org/hco/8/GRCh38#67017866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10073710-C-A

67021185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10076218-A-G

67021231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10076264-A-T

67021510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10076710-C-T

67021660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10076893-C-T

67021666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10076899-C-T

67022299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10077786-G-C

http://identifiers.org/hco/8/GRCh38#67022366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10077854-A-C

http://identifiers.org/hco/8/GRCh38#67027099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10078170-C-A

67027099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078170-C-G

67027130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078216-A-G

67027144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078235-G-A

67027144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078235-G-T

67027151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078242-T-C

http://identifiers.org/hco/8/GRCh38#67027188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10078278-A-C

67027427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078535-T-C

67027607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078694-A-G

67027773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10078868-T-C

67028436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10079261-A-G

67028492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 10079298-G-A

67028509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10079313-G-A

67028610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079407-A-G

67028611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079408-G-A

67028611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079408-G-C

67028611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079408-G-T

67028650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079450-G-T

67028696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079501-G-A

67028696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10079501-G-T

67028789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10079527-C-G

67029030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10079721-G-A

67030469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080500-C-G

67030524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080551-G-A

67030640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080656-G-A

67030640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080656-G-C

http://identifiers.org/hco/8/GRCh38#67030794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10080831-C-A

67030794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080831-C-T

67030834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080854-A-G

67030834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080854-A-T

67030844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080862-A-G

67030939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10080954-G-A

67032074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082026-T-G

67032389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082327-A-G

67032389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082327-A-T

67032531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082486-G-C

67032636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082596-A-G

67032682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082647-C-T

67032720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082685-C-G

67032965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082927-T-A

67033035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10082995-G-C

67033545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10083440-G-A

67033718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10083614-C-G

67034164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10083810-G-A

67034606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084142-T-C

67034853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084383-C-G

67035031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084543-C-T

67035612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084617-T-A

67035612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084617-T-C

67035612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084617-T-G

67035620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084625-T-A

67035620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084625-T-C

http://identifiers.org/hco/8/GRCh38#67035643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10084646-C-A

67035855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084853-T-A

67035892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084895-T-A

67035969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10084961-G-T

67036191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10085215-T-A

67036250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10085452-G-A

67037464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10087441-A-G

67037609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 10087572-G-A

67037693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10087639-A-G

67037737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10087679-G-T

67037763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10087705-T-C

67038144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10088345-G-A

67038144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10088345-G-T

67038319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10088528-A-T

67038357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10088566-T-C

67038671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10088813-T-C

67038771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10088912-C-T

67038876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10089008-T-A

67038876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10089008-T-C

67039197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10089334-T-C

67039379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10089500-T-A

67039385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10089510-T-C

67042531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10094500-C-G

67042531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10094500-C-T

67042732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10094677-T-G

67043033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10095016-A-G

67043036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10095019-A-G

http://identifiers.org/hco/8/GRCh38#67043048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10095024-C-A

67043048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10095024-C-T

http://identifiers.org/hco/8/GRCh38#67043056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#10095032-C-A

67043056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 10095032-C-G

http://identifiers.org/hco/8/GRCh38#67043102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#10095076-C-A

67043102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095076-C-T

http://identifiers.org/hco/8/GRCh38#67043161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#10095133-A-C

67043161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095133-A-G

67043167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095139-T-C

67043172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095144-A-T

67043242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 10095213-G-A

67043242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095213-G-T

67043252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095223-T-C

67043305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 10095276-G-A

67043305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 10095276-G-C

67043305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 10095276-G-T

67043383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095358-G-T

67043387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095363-C-T

67043455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10095415-T-C

http://identifiers.org/hco/8/GRCh38#67045524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#10097059-C-A

67045537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10097072-T-C

67045552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10097086-G-T

67045691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10097225-T-G

67045697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10097231-A-G

67045779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 10097301-G-A

67045844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 10097360-T-C

67045937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 10097453-C-T

http://identifiers.org/hco/8/GRCh38#67046046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#10097692-C-A

67046090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10097923-T-A

67046244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10098063-G-T

67046280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10098098-C-T

67050893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10100342-A-G

http://identifiers.org/hco/8/GRCh38#67051087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#10100474-C-A

http://identifiers.org/hco/8/GRCh38#67051361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#10100954-A-C

67051410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10101001-G-T

67051480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10101049-G-T

67051490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 10101061-G-A

67056511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 10102556-T-A

67056511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 10102556-T-C

67056533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 10102578-A-G

67056554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 10102599-A-G

67056557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 10102602-T-C

67056560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 10102605-A-G

67056581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 10102626-T-C

67056590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33732
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 10102635-A-G