http://identifiers.org/hco/8/GRCh38#8317737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#36614963-C-A

8317839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614855-A-G

8317911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36614781-A-G

8317929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614753-G-A

8317929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614753-G-C

8317929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614753-G-T

8317956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614731-G-A

8317956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614731-G-C

8317956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614731-G-T

8317995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614695-T-C

8318047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36614662-A-G

8318185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614538-A-G

8318203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614520-G-A

8318251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614472-C-G

8318251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614472-C-T

8318293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614430-A-G

8318332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614391-C-T

8318347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614376-G-A

8318347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36614376-G-T

8318349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36614374-G-A

8318349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36614374-G-C

8318349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36614374-G-T

http://identifiers.org/hco/8/GRCh38#8318425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36614298-C-A

8318425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614298-C-T

8318464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614259-G-A

8318464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614259-G-T

8318479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614244-C-T

8318602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36614121-C-T

http://identifiers.org/hco/8/GRCh38#8318767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#36613956-C-A

8318767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36613956-C-T

8318819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36613928-G-A

8318819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36613928-G-C

8318819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36613928-G-T

http://identifiers.org/hco/8/GRCh38#8318894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36613865-C-A

8318894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613865-C-G

8318894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613865-C-T

8318911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613848-T-A

8318911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613848-T-C

8318911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613848-T-G

8318995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36613764-A-T

8319012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36613747-G-A

8319012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36613747-G-C

8319154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613605-G-T

http://identifiers.org/hco/8/GRCh38#8319220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36613536-C-A

8319220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36613536-C-T

8319335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613421-G-A

8319335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613421-G-C

8319335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613421-G-T

8319395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613337-G-A

8319395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613337-G-T

8319431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613300-T-A

8319431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36613300-T-C

8320309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36612521-G-C

8320364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612465-T-C

8320415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36612409-G-T

8320914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36611881-A-G

8321007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611789-T-C

8321082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611725-C-T

8321212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611586-G-A

8321542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611326-T-C

8321547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611320-G-C

8321560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611266-G-A

8321560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611266-G-C

8321560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611266-G-T

http://identifiers.org/hco/8/GRCh38#8321563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36611263-C-A

8321563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611263-C-G

8321594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611231-G-C

8321784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36611047-T-C

8321832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36611009-T-C

8321862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36610979-T-C

8321865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36610976-T-C

8321871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36610970-G-A

http://identifiers.org/hco/8/GRCh38#8321982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36610874-C-A

8321982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610874-C-T

8323822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610565-G-T

http://identifiers.org/hco/8/GRCh38#8323846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36610541-A-C

8323982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610406-T-C

http://identifiers.org/hco/8/GRCh38#8323998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36610390-C-A

8324049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610356-A-G

8324059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610346-C-G

http://identifiers.org/hco/8/GRCh38#8324123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36610288-C-A

8324153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610265-G-T

8324285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610125-T-A

8324285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36610125-T-C

8324489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609931-C-T

8324683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609754-G-A

8324895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609575-G-T

8324982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609490-T-A

8325032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609447-G-C

8325220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609267-C-T

8325234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609259-C-G

8325234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609259-C-T

8325241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609252-A-G

8325372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609135-C-G

8325372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609135-C-T

8325485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36609020-C-T

http://identifiers.org/hco/8/GRCh38#8325540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36608969-A-C

8327714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36607260-A-G

http://identifiers.org/hco/8/GRCh38#8327740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36607234-A-C

http://identifiers.org/hco/8/GRCh38#8327780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36607194-C-A

8327780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36607194-C-G

8328007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36606967-C-G

8328007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36606967-C-T

http://identifiers.org/hco/8/GRCh38#8328040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36606934-C-A

8328040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36606934-C-G

8328040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36606934-C-T

8328052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36606922-G-A

8328052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36606922-G-C

http://identifiers.org/hco/8/GRCh38#8328153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36606821-A-C

8328153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606821-A-G

8328168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606806-G-C

http://identifiers.org/hco/8/GRCh38#8328202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36606772-A-C

8328209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606765-T-A

8328351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36606617-G-A

8328351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606617-G-C

8328351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606617-G-T

8328389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606576-G-A

8328407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606558-G-A

8328407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606558-G-T

8328440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36606525-T-G

http://identifiers.org/hco/8/GRCh38#8328468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36606497-A-C

8328522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606445-G-A

8328522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606445-G-T

8328525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606442-G-C

8328525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36606442-G-T

8330420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36605003-T-A

8330519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604869-G-A

8330527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604861-G-A

8330555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604833-G-A

8330621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604784-C-T

8330681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604724-G-T

http://identifiers.org/hco/8/GRCh38#8330980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36604418-C-A

8330980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604418-C-T

8331268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604153-T-A

8331286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604138-T-C

8331291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36604129-C-G

8331676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603829-T-C

8331826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603695-T-C

8331826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603695-T-G

8331885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603639-G-A

8331896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603628-G-C

8332180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603374-T-G

8332644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603048-G-A

8332644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603048-G-C

8332650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603042-T-C

8332658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36603034-T-C

8332718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602975-T-G

8332843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602881-G-A

8332871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602856-G-C

8333024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602692-T-C

8333361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602374-G-A

8333516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602224-G-C

http://identifiers.org/hco/8/GRCh38#8333532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36602208-C-A

http://identifiers.org/hco/8/GRCh38#8333643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36602098-C-A

8333643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602098-C-T

8333647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602094-C-T

8333655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602089-G-C

8333744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36602002-T-C

8333769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601977-A-G

8334446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601492-A-G

8334583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601337-C-G

8334605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601315-G-A

8334696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601228-C-T

8334736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601188-A-G

8334783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36601140-A-G

8335222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600954-T-A

8335442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600745-T-G

8335480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600715-G-T

http://identifiers.org/hco/8/GRCh38#8335584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36600603-A-C

http://identifiers.org/hco/8/GRCh38#8335604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36600581-A-C

8335610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600575-A-G

8335700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600483-G-T

8335736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36600414-T-C

http://identifiers.org/hco/8/GRCh38#8335827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36600168-C-A

8335975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599876-T-G

8336119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599753-T-G

8336211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599680-C-G

8336246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599663-A-G

8336422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599360-T-G

8336468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599296-G-A

8336496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36599274-G-A

http://identifiers.org/hco/8/GRCh38#8336871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36598952-C-A

8336894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598929-T-A

8336894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598929-T-C

8336894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598929-T-G

8337001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598852-C-G

8337061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598795-G-A

http://identifiers.org/hco/8/GRCh38#8337104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36598751-A-C

8337107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598748-G-A

8337122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598735-G-C

8337300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598588-A-G

8337342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598547-T-C

8337525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598280-T-C

8337550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598261-C-G

8337550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598261-C-T

8337617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598200-G-C

8337747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598079-C-T

8337791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36598046-C-G

8337875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597972-C-T

http://identifiers.org/hco/8/GRCh38#8337956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36597896-A-C

8337971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597882-C-T

8338153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597719-A-G

8338265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597631-C-T

8338375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597541-T-A

8338456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597458-A-G

8338459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597455-T-A

8338759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597212-A-G

8338827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597150-C-T

8338891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597105-A-G

8338903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597092-T-C

8338903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597092-T-G

8338932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597063-A-G

8338997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36597000-T-C

8339058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596938-G-A

8339162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596662-G-T

8339419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596364-G-A

8339419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596364-G-T

8339447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596339-T-C

8339450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596336-G-A

8339450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596336-G-C

http://identifiers.org/hco/8/GRCh38#8339451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36596335-C-A

8339451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596335-C-T

8339458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596328-G-A

8339600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36596191-A-T

8339606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36596185-G-A

8339606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36596185-G-C

http://identifiers.org/hco/8/GRCh38#8339705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36596091-C-A

8339705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596091-C-T

http://identifiers.org/hco/8/GRCh38#8339728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36596068-A-C

8339739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596057-G-A

8339739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36596057-G-T

8339842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595963-G-A

8339973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595839-A-G

8340015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595772-C-T

8340284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595520-G-C

8340350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595456-A-G

8340415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595389-G-C

8340415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595389-G-T

8340433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595371-T-C

8340457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36595348-C-G

8345914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590491-G-A

8345973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590432-G-C

8346048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590345-C-T

8346201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590210-A-G

8346236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36590144-A-T

8346428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589984-A-T

8346453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589959-C-T

8346454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589958-T-C

8346555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589855-T-C

8346683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589729-A-G

8346762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589656-G-T

8346784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589634-T-C

http://identifiers.org/hco/8/GRCh38#8346859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36589561-C-A

8346859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589561-C-T

8346950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589471-T-C

8347016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589403-A-G

8347236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589191-G-T

8347272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589156-G-T

8347299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36589134-C-T

8347494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588969-C-T

8347573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588891-T-C

http://identifiers.org/hco/8/GRCh38#8347673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36588789-A-C

http://identifiers.org/hco/8/GRCh38#8347731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36588704-C-A

8347767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588670-C-T

8348305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588536-C-T

8348328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36588513-C-T

8348513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36587464-T-C

8348590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36587393-G-C

8349665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36586658-A-G

8350384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585329-A-G

8350452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585268-C-T

8350510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585225-G-A

8350676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36585088-C-G

8351677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584589-G-C

http://identifiers.org/hco/8/GRCh38#8351953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36584300-A-C

http://identifiers.org/hco/8/GRCh38#8351979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36584271-A-C

8351979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584271-A-G

8351983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584267-G-A

8351983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584267-G-T

8352052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584226-C-T

8352116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584135-A-G

8352173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36584066-A-G

8352339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36583916-T-G

8363843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581792-G-A

8363843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581792-G-C

8363873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581761-G-C

8363970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581666-C-G

8364058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581574-T-C

8364065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581567-G-C

8364106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581527-G-C

8364178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581426-T-A

8364178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581426-T-C

8364300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36581339-G-A

8364679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580963-G-C

8364679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580963-G-T

8364823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580815-C-T

http://identifiers.org/hco/8/GRCh38#8364838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36580800-C-A

8364898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36580751-A-G

http://identifiers.org/hco/8/GRCh38#8364941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36580696-A-C

8365047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579877-G-T

8365257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579712-T-C

8365257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579712-T-G

8365264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579705-T-A

8365267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579702-C-T

8365270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579699-C-G

8365270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579699-C-T

http://identifiers.org/hco/8/GRCh38#8365271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36579698-C-A

8365271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579698-C-T

8365290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579679-C-G

8365308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579661-C-T

8366046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579594-G-C

8366110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579531-T-C

8366125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579516-T-C

8366216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579430-G-A

8366286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36579362-C-T

http://identifiers.org/hco/8/GRCh38#8367119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

8367189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

8367205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

8367606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578943-C-G

8367613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578936-T-A

8367613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578936-T-G

8367627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578922-G-A

8367948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578911-G-C

8367984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578874-G-A

8367998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578861-C-T

8368088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578771-T-C

http://identifiers.org/hco/8/GRCh38#8368107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36578618-A-C

8368282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578066-T-C

8368309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578036-G-A

8368309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36578036-G-C

8368377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577966-C-T

8368386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577957-C-T

8368387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577956-G-A

8368387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577956-G-C

8368441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577903-T-C

8368508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577834-G-T

http://identifiers.org/hco/8/GRCh38#8368907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36577474-C-A

8369011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577346-A-G

8369111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577255-G-A

8369111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577255-G-C

8369111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36577255-G-T

8369205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576629-A-T

http://identifiers.org/hco/8/GRCh38#8369341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36576501-C-A

8369893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576179-G-T

8369899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576173-G-A

8369970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576076-G-A

8369990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36576056-G-A

8370095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575953-T-C

8370193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575777-T-C

8370211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575759-C-T

8370285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575688-C-G

8370285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575688-C-T

8370447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575530-T-C

8370699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575293-T-C

8370730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36575261-C-T

http://identifiers.org/hco/8/GRCh38#8371956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#36574987-C-A

8371975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574972-G-A

8371975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574972-G-C

8371975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574972-G-T

8371991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36574956-C-T

8372023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574928-G-A

8372131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574818-C-T

8372132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574817-G-A

8372168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574781-A-T

8372196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574753-T-C

8372209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574739-T-G

8372317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574691-G-C

8372318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574690-C-T

8372341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574683-C-T

8372353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574678-A-G

8372431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574594-T-C

8372521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574512-G-C

http://identifiers.org/hco/8/GRCh38#8372799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36574321-A-C

8372828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574303-G-A

8372935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574251-G-C

8372974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574215-G-C

8373144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36574064-T-C

8373537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573908-C-T

8373675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573794-A-T

8373825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36573713-C-G

8374540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572935-G-T

8374549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572926-T-C

8374552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572923-C-T

http://identifiers.org/hco/8/GRCh38#8374642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36572846-A-C

8374643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572845-G-A

8374665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572828-C-G

8374665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572828-C-T

http://identifiers.org/hco/8/GRCh38#8374816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36572666-C-A

8374927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572558-G-T

8374961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572526-C-T

http://identifiers.org/hco/8/GRCh38#8375026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36572466-C-A

8375026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572466-C-G

8375026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572466-C-T

8375057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572432-A-G

http://identifiers.org/hco/8/GRCh38#8375069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36572420-C-A

8375069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572420-C-T

8375153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572344-T-C

8375553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36572259-T-G

http://identifiers.org/hco/8/GRCh38#8375831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36572171-A-C

8375831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572171-A-G

8375848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572154-C-T

8375894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572111-G-C

http://identifiers.org/hco/8/GRCh38#8375913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36572094-C-A

8375980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36572021-C-T

8376361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36571389-T-C

8376582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36571168-T-A

http://identifiers.org/hco/8/GRCh38#8376588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36571162-A-C

http://identifiers.org/hco/8/GRCh38#8376589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36571161-C-A

http://identifiers.org/hco/8/GRCh38#8376658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36571089-C-A

8376658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36571089-C-G

http://identifiers.org/hco/8/GRCh38#8376682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36571065-C-A

8376766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36570999-A-T

8376795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36570970-G-C

8376848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570917-G-C

8376848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570917-G-T

8376976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570789-G-A

http://identifiers.org/hco/8/GRCh38#8376988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36570777-A-C

8376988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570777-A-T

8377091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 36570668-G-A

8377091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570668-G-T

8377251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36570508-G-A

8377251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36570508-G-C

8377251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36570508-G-T

8377303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570456-A-T

8377318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570441-T-C

8377339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570420-A-T

8377447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570321-G-A

8377547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570221-A-G

8377635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36570145-G-C

8377801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36569961-G-A

8377801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36569961-G-T

8378080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 36569706-T-C

http://identifiers.org/hco/8/GRCh38#8378082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36569704-C-A

8378082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36569704-C-T

8378119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36569651-T-C

8378461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36569338-C-T

8378917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36569026-G-C

http://identifiers.org/hco/8/GRCh38#8379371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36568758-C-A

8379527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36568619-G-A

8379687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36568465-C-G

8379890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36568254-T-C

8379978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36568150-T-C

8379984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36568144-T-C

8380978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567585-C-T

8381003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567559-G-A

8381032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567532-T-C

8381097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567468-T-G

8381212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567361-G-T

8381298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567260-G-A

8381298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36567260-G-T

http://identifiers.org/hco/8/GRCh38#8381345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#36567212-C-A

http://identifiers.org/hco/8/GRCh38#8381378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#36567179-C-A

8381378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36567179-C-T

8381394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36567163-A-G

8381458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36567099-T-A

8381458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36567099-T-C

8381616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 36566941-G-A

8381629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 36566928-T-G

8381760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36566797-G-A

8381760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36566797-G-C

8381760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36566797-G-T

8381761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36566796-G-A

8381761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36566796-G-C

8381811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36566745-A-G

8381866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566692-A-G

8381887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566677-G-C

8381887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566677-G-T

8381916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566642-G-T

8381917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566641-A-G

8381968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566581-G-A

8381968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566581-G-C

8381983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566566-T-G

8382035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566512-A-G

http://identifiers.org/hco/8/GRCh38#8382050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36566497-C-A

8382158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566273-C-T

8382173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566096-G-A

8382209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36566056-C-T

8382279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565995-T-C

8382325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565942-G-A

http://identifiers.org/hco/8/GRCh38#8382371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36565896-C-A

http://identifiers.org/hco/8/GRCh38#8382565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36565696-A-C

8382668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565614-T-A

8382764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565519-A-G

8382781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565501-C-G

8382791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565491-G-A

8382935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565237-G-A

8383142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36565037-G-A

8384054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564408-A-G

8384133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564346-G-C

http://identifiers.org/hco/8/GRCh38#8384144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36564335-C-A

8384144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564335-C-G

http://identifiers.org/hco/8/GRCh38#8384293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36564213-C-A

8384302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564132-G-A

8384314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564117-G-A

8384362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36564064-G-C

http://identifiers.org/hco/8/GRCh38#8384441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36563986-C-A

8384470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563964-G-A

8384470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563964-G-C

http://identifiers.org/hco/8/GRCh38#8384473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#36563961-A-C

8384520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36563916-C-T

8384545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563891-C-G

8384587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36563849-G-T

http://identifiers.org/hco/8/GRCh38#8385285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36563212-C-A

http://identifiers.org/hco/8/GRCh38#8385328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36563175-A-C

8385421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36563103-C-G

8385421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36563103-C-T

8385471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36563040-G-A

8385473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36563038-T-G

8386177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36562298-C-T

http://identifiers.org/hco/8/GRCh38#8386229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36562231-C-A

8386229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 36562231-C-T

http://identifiers.org/hco/8/GRCh38#8386351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36562110-C-A

8386351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36562110-C-T

http://identifiers.org/hco/8/GRCh38#8386403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#36562049-C-A

8386403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25438
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36562049-C-T