233833464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88187940-T-C

233833464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88187940-T-G

233833475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88187952-G-T

http://identifiers.org/hco/2/GRCh38#233833513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88187978-C-A

233833513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88187978-C-T

http://identifiers.org/hco/2/GRCh38#233833587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88188014-C-A

233833587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88188014-C-T

http://identifiers.org/hco/2/GRCh38#233833590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#88188017-C-A

233833598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 88188025-A-G

233833609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 88188035-G-A

233833609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 88188035-G-T

http://identifiers.org/hco/2/GRCh38#233833631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88188057-C-A

233833631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88188057-C-T

233833652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88188075-A-T

http://identifiers.org/hco/2/GRCh38#233833659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88188084-C-A

http://identifiers.org/hco/2/GRCh38#233833671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88188096-C-A

http://identifiers.org/hco/2/GRCh38#233833677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88188102-C-A

233833677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88188102-C-G

http://identifiers.org/hco/2/GRCh38#233837976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88191259-A-C

233838049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191311-C-G

233838049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191311-C-T

233838058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191320-G-A

233838058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191320-G-C

233838324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191580-G-A

233838324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191580-G-T

233838365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191621-G-A

233838373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88191629-T-G

http://identifiers.org/hco/2/GRCh38#233840540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88192819-C-A

233840540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192819-C-T

233840555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192830-T-G

233840592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192874-A-T

233840600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192882-C-G

233840600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192882-C-T

233840604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192886-C-G

233840604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88192886-C-T

233840609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 88192891-C-T

233840624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192897-G-A

233840627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192900-T-C

233840634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192907-A-G

233840685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192932-C-G

233840685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192932-C-T

http://identifiers.org/hco/2/GRCh38#233840686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88192933-C-A

233840690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192937-G-A

http://identifiers.org/hco/2/GRCh38#233840692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88192939-A-C

233840729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192976-C-T

233840733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192980-G-A

233840733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88192980-G-T

233840742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88192989-C-T

233840754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193001-G-T

233840755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193002-G-A

http://identifiers.org/hco/2/GRCh38#233840817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88193031-C-A

233840955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193166-T-C

233840956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193167-A-G

233841033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193241-C-G

233841033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193241-C-T

233841084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193292-C-T

http://identifiers.org/hco/2/GRCh38#233841126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88193334-A-C

233841180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193382-T-C

233841180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193382-T-G

233841192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193394-T-A

233841241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193434-C-T

233841313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193512-G-A

233841378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193577-T-C

233841384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193583-T-C

233841384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193583-T-G

http://identifiers.org/hco/2/GRCh38#233841419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88193618-C-A

233841419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193618-C-T

233841450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193649-C-T

233841503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193702-T-C

233841564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193763-T-A

http://identifiers.org/hco/2/GRCh38#233841569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88193768-A-C

233841725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193897-C-T

233841745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193917-A-G

233841759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193931-T-C

233841782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193954-C-T

233841784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193956-T-C

233841790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: synonymous variant
orthologous variants: 88193962-A-G

233841791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: missense variant
orthologous variants: 88193963-G-A

233841894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88194072-T-G

233842108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88194283-G-A

233842130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88194305-G-A

233842130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88194305-G-C

233842162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88194337-C-T

233842163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88194338-G-A

233842163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88194338-G-T

233842246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88194418-T-C

233842255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88194430-A-G

233842275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88194450-G-A

233842275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88194450-G-T

233842403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88194564-G-A

233842459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88194616-T-G

233843640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195102-C-T

233843699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195145-C-T

233843720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195165-T-C

http://identifiers.org/hco/2/GRCh38#233843907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88195369-A-C

233844037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195520-A-G

233844063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195553-A-G

233844113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195601-G-A

233844113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195601-G-T

233844134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195618-G-A

http://identifiers.org/hco/2/GRCh38#233844140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88195624-C-A

233844140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195624-C-T

233844160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195637-T-C

233844171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195648-C-T

233844220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88195685-C-G

233844403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195872-T-A

233844404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195873-G-A

233844404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195873-G-T

233844412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88195882-G-T

233844589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196026-A-G

233844613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196050-G-A

233844717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196146-G-C

233844748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196169-G-A

233844787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196207-C-T

233844800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196220-C-T

233844805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196222-A-G

http://identifiers.org/hco/2/GRCh38#233844911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88196329-C-A

http://identifiers.org/hco/2/GRCh38#233845502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88196828-C-A

233845502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196828-C-T

233845507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196833-C-G

233845649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196973-A-G

233845663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88196986-T-C

233845686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88197007-T-C

233845705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88197025-C-T

233845759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88197074-T-C

233845808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 88197123-G-A

233845833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197147-G-T

233845860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197169-G-A

233845860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197169-G-C

233845860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197169-G-T

233845886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197200-G-T

233845972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197268-A-G

233845989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197299-T-C

233845997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197307-T-C

233846007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197323-G-A

233846007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197323-G-T

http://identifiers.org/hco/2/GRCh38#233846022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88197338-C-A

233846069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88197396-T-C

http://identifiers.org/hco/2/GRCh38#233846093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88197420-A-C

http://identifiers.org/hco/2/GRCh38#233849625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88200274-C-A

http://identifiers.org/hco/2/GRCh38#233849650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88200300-C-A

233849654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200304-G-T

233849699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200352-T-C

233849700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200353-T-G

233849717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200371-A-T

233849737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200389-A-G

233849737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200389-A-T

233849748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200397-G-A

233849748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200397-G-C

233849748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88200397-G-T

http://identifiers.org/hco/2/GRCh38#233849762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88200411-C-A

233849762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 88200411-C-T

233849800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 88200452-A-G

233849843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88200486-G-A

233849843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 88200486-G-T

http://identifiers.org/hco/2/GRCh38#233849905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88200524-C-A

233849905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88200524-C-G

233849905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88200524-C-T

http://identifiers.org/hco/2/GRCh38#233850000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88200603-A-C

http://identifiers.org/hco/2/GRCh38#233850004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88200605-C-A

233850509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201037-T-C

233850570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201071-G-A

233850587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201079-G-A

233850647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201119-G-A

233850647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201119-G-T

233850766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201206-G-C

233850802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201237-G-A

233851005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201418-T-C

233851260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201643-C-T

233851296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88201658-G-A

http://identifiers.org/hco/2/GRCh38#233851752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88202039-C-A

233851839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202126-G-A

233851882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202168-T-C

233852083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202325-C-T

233852084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202326-G-A

233852107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202356-A-G

233852445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202650-G-A

233852445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202650-G-C

233852445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202650-G-T

233852451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202656-G-T

233852452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202658-T-C

http://identifiers.org/hco/2/GRCh38#233852457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88202663-C-A

233852457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202663-C-T

233852458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202664-G-A

233852458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202664-G-T

http://identifiers.org/hco/2/GRCh38#233852471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88202687-C-A

233852471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202687-C-T

233852484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202698-G-T

http://identifiers.org/hco/2/GRCh38#233852526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88202734-C-A

233852526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202734-C-T

233852529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202737-C-T

233852540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202743-G-A

233852540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202743-G-T

233852541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 88202744-G-T

233852573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 88202772-C-T

233852647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202841-T-C

233852659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202856-T-C

233852667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202865-G-A

233852667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202865-G-T

233852688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202886-T-A

233852688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202886-T-C

233852688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202886-T-G

233852694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202892-G-A

233852694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202892-G-C

233852694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202892-G-T

http://identifiers.org/hco/2/GRCh38#233852712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88202912-A-C

233852712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202912-A-G

233852727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202926-T-A

233852727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202926-T-C

233852727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202926-T-G

233852757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88202953-T-C

233852899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88203106-C-T

233852962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88203152-G-A

233852982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88203168-A-G

http://identifiers.org/hco/2/GRCh38#233853045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88204280-A-C

233853056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204291-G-A

233853056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204291-G-T

http://identifiers.org/hco/2/GRCh38#233853349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88204545-C-A

233853349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204545-C-G

233853413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204586-G-A

233853425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204607-G-C

http://identifiers.org/hco/2/GRCh38#233853510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88204687-A-C

http://identifiers.org/hco/2/GRCh38#233853587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88204751-C-A

233853587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204751-C-T

233853776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204874-G-A

233853776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204874-G-C

233853776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204874-G-T

233853793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204889-C-T

233853805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204901-T-C

233853810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204907-A-G

http://identifiers.org/hco/2/GRCh38#233853813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88204910-C-A

233853813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204910-C-T

233853840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88204937-T-C

233853856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88204953-C-G

233853870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88204967-G-A

http://identifiers.org/hco/2/GRCh38#233853884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88204981-C-A

233853884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88204981-C-G

233853885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88204982-G-A

233853885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88204982-G-C

233853915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 88205012-G-A

233853918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 88205015-G-A

http://identifiers.org/hco/2/GRCh38#233853945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88205038-A-C

233853945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88205038-A-G

233854346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88205043-G-A

233854346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88205043-G-T

233854420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88205132-G-A

233854423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88205135-G-A

233854432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88205144-C-T

233854444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 88205156-C-T

http://identifiers.org/hco/2/GRCh38#233854482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88205194-C-A

233854482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88205194-C-T

233854485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88205197-G-A

233854485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 88205197-G-T

http://identifiers.org/hco/2/GRCh38#233854495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88205212-C-A

233854495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88205212-C-G

233854495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 88205212-C-T

http://identifiers.org/hco/2/GRCh38#233854525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88205229-C-A

http://identifiers.org/hco/2/GRCh38#233854530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88205234-C-A

233854530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88205234-C-G

233854530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 88205234-C-T

http://identifiers.org/hco/2/GRCh38#233854562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#88205247-A-C

233854562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5 prime UTR variant
orthologous variants: 88205247-A-G

233854562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25444
most severe consequence: 5 prime UTR variant
orthologous variants: 88205247-A-T