237324085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90694654-T-A

237324159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90694729-C-T

237324174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90694745-C-T

http://identifiers.org/hco/2/GRCh38#237324275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90694839-C-A

http://identifiers.org/hco/2/GRCh38#237324283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90694847-C-A

237324283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90694847-C-G

http://identifiers.org/hco/2/GRCh38#237324464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90694996-C-A

237324464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90694996-C-G

237324464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90694996-C-T

http://identifiers.org/hco/2/GRCh38#237324575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90695107-C-A

237324575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90695107-C-T

237324585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90695116-G-A

237324585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 90695116-G-T

237324631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90695162-A-T

237324802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90695331-G-A

237324802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90695331-G-C

237324827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695356-A-G

237324862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695390-G-A

237324862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695390-G-T

237324878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695406-A-G

237324902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695430-G-C

237324902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695430-G-T

237324912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695440-T-A

237324912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695440-T-C

http://identifiers.org/hco/2/GRCh38#237324917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90695445-C-A

237324917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695445-C-G

237324917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695445-C-T

237325022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695516-T-A

237325022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695516-T-G

237325188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695594-A-G

237325253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90695655-C-T

http://identifiers.org/hco/2/GRCh38#237325403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90695847-C-A

237325403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695847-C-T

237325434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695906-G-A

237325434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695906-G-T

http://identifiers.org/hco/2/GRCh38#237325461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90695931-A-C

237325461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90695931-A-G

237325609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90696095-G-A

http://identifiers.org/hco/2/GRCh38#237325663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#90696149-A-C

237325663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90696149-A-G

237325704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90696190-C-T

http://identifiers.org/hco/2/GRCh38#237325711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90696197-C-A

237325715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90696201-T-C

237325756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696242-T-A

237325756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696242-T-C

237325770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696256-T-C

http://identifiers.org/hco/2/GRCh38#237325787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90696279-C-A

237325787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696279-C-T

http://identifiers.org/hco/2/GRCh38#237325883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90696363-C-A

http://identifiers.org/hco/2/GRCh38#237325890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90696370-C-A

237325890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696370-C-T

237325913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696393-A-G

http://identifiers.org/hco/2/GRCh38#237326049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90696500-C-A

237326049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696500-C-G

237326051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696502-A-G

237326136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696567-T-G

237326315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696795-A-T

237326363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696941-G-A

237326363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696941-G-T

237326364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696942-G-A

237326364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696942-G-T

237326388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90696966-A-G

237326425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697003-G-A

http://identifiers.org/hco/2/GRCh38#237326444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90697022-C-A

237326444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697022-C-T

237326448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697026-C-T

237326464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697042-G-A

237326464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697042-G-T

237326607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697185-T-C

237326665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697241-T-C

237326666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90697242-G-T

237330388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697358-A-G

237330389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697359-C-T

237330462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697430-G-T

237330536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697494-T-C

237331916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697768-G-T

http://identifiers.org/hco/2/GRCh38#237331939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90697791-C-A

237331939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697791-C-T

237331943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697795-A-G

237332150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90697919-C-G

237332566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90699046-G-A

237332594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90699074-C-G

http://identifiers.org/hco/2/GRCh38#237333133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90700327-C-A

237333133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700327-C-T

http://identifiers.org/hco/2/GRCh38#237333136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90700330-C-A

237333194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700390-T-C

237333197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700393-G-A

237333197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700393-G-T

237333232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700428-T-A

237333232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700428-T-C

http://identifiers.org/hco/2/GRCh38#237333270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90700467-C-A

237333270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700467-C-G

237333270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700467-C-T

237333356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90700554-C-T

237334449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701003-A-G

237334481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701035-T-C

237334481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701035-T-G

http://identifiers.org/hco/2/GRCh38#237334687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90701220-C-A

237334726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90701259-G-A

237334771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90701304-A-G

http://identifiers.org/hco/2/GRCh38#237334823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90701356-C-A

http://identifiers.org/hco/2/GRCh38#237334888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90701421-A-C

237334888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 90701421-A-G

237334901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701430-A-T

237334925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701456-A-G

237334971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701502-G-A

237334971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701502-G-C

237335015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701544-G-A

237335015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701544-G-T

237335040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701567-C-G

237335140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701676-T-C

http://identifiers.org/hco/2/GRCh38#237335339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90701886-C-A

237335354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701901-C-T

237335439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90701984-A-G

237335713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90702228-G-A

237336168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90703286-C-T

http://identifiers.org/hco/2/GRCh38#237336181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90703296-C-A

237336263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90703375-G-A

237336328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90703428-G-A

237336328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90703428-G-C

237336362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90703879-G-A

237336362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90703879-G-C

237336362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90703879-G-T

237336419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -G-A

237336431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -A-G

237336617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704088-T-C

237336759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704221-C-T

237336845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704311-T-C

237336880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704342-C-T

237338827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704984-G-A

237338827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704984-G-T

http://identifiers.org/hco/2/GRCh38#237338839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90704996-A-C

237338839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90704996-A-G

http://identifiers.org/hco/2/GRCh38#237339077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90705225-C-A

237339077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90705225-C-G

237339077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90705225-C-T

237339835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90705862-A-T

237340029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706011-G-A

237340136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706118-A-G

237340152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706134-T-C

237340167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706149-G-A

237340221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706202-T-C

237340256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706236-A-T

http://identifiers.org/hco/2/GRCh38#237340318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90706333-C-A

237340318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706333-C-G

237340318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706333-C-T

http://identifiers.org/hco/2/GRCh38#237340360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90706374-C-A

237340360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706374-C-T

http://identifiers.org/hco/2/GRCh38#237340361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90706375-A-C

237340361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706375-A-G

237340428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706454-C-T

237340434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90706460-G-A

237340495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90706521-C-T

237340501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90706527-G-A

237340555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90706581-G-A

237340768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90706794-G-A

237340768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90706794-G-T

237340831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90706857-C-G

237341074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90707100-G-A

237341074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90707100-G-C

237341074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90707100-G-T

237341137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90707163-G-A

237341137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90707163-G-C

237341232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707246-G-A

http://identifiers.org/hco/2/GRCh38#237341952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90707606-A-C

237342007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707647-G-A

237342007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707647-G-T

237342008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707648-G-T

237342027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707667-G-T

237342033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707673-G-A

237342033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90707673-G-T

http://identifiers.org/hco/2/GRCh38#237342210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90707850-A-C

237342210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90707850-A-G

237342219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90707856-A-T

http://identifiers.org/hco/2/GRCh38#237342294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90707917-C-A

237342301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90707924-T-C

237342479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90707974-A-G

237342504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90707998-A-G

237342514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708009-T-A

237342514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708009-T-C

http://identifiers.org/hco/2/GRCh38#237342601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708108-C-A

http://identifiers.org/hco/2/GRCh38#237342620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708126-C-A

237342620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708126-C-T

237342622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708128-G-C

237342622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708128-G-T

237343050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708483-T-C

237343055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708488-G-T

237343076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708501-G-T

237343090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708515-T-C

237343097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708522-A-G

237343105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708532-G-A

237343105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708532-G-T

http://identifiers.org/hco/2/GRCh38#237343133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708566-C-A

237343133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708566-C-T

http://identifiers.org/hco/2/GRCh38#237343144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708577-C-A

http://identifiers.org/hco/2/GRCh38#237343145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708578-C-A

http://identifiers.org/hco/2/GRCh38#237343172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708605-C-A

237343622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708667-G-T

237343627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708672-T-A

237343627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708672-T-C

http://identifiers.org/hco/2/GRCh38#237343629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708674-C-A

237343629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708674-C-T

237343687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708731-T-C

237343692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708737-G-A

237343692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708737-G-C

237343692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708737-G-T

237343693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90708738-G-T

http://identifiers.org/hco/2/GRCh38#237343783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708848-C-A

237343783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708848-C-T

237343820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708869-G-T

http://identifiers.org/hco/2/GRCh38#237343838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90708887-C-A

237343838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708887-C-T

237343853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708902-C-G

237343895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90708944-G-T

237343970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709010-G-C

237343970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709010-G-T

237343995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709026-G-T

http://identifiers.org/hco/2/GRCh38#237344021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90709040-C-A

237344022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709041-A-G

237344028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709047-T-C

237344034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709053-A-G

237344061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709085-T-G

237344103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709119-G-A

237344103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709119-G-T

http://identifiers.org/hco/2/GRCh38#237344104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90709120-C-A

237344104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709120-C-T

237344109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709125-G-T

237344141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709157-G-T

http://identifiers.org/hco/2/GRCh38#237344178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90709197-C-A

237344178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709197-C-T

237344256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709270-G-A

237344256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709270-G-T

237344266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90709283-C-T

237344362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90709369-G-C

http://identifiers.org/hco/2/GRCh38#237344410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90709417-C-A

237344410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90709417-C-T

http://identifiers.org/hco/2/GRCh38#237344480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90709487-A-C

237344481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90709488-C-T

237344482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90709489-A-G

237344686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90709693-C-G

237344686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90709693-C-T

237344698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90709705-T-C

237344866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90709866-G-A

237344942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 90709940-G-A

237344980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90709978-G-A

237345000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90709998-G-A

http://identifiers.org/hco/2/GRCh38#237345005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90710003-A-C

237345029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710028-T-C

237345089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90710094-A-G

237345147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710148-G-A

237345147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710148-G-C

237345147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710148-G-T

237345169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710169-C-T

237345231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710231-G-A

237345514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710716-T-G

237345554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710785-T-G

237345563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710794-C-G

237345607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90710852-G-A

http://identifiers.org/hco/2/GRCh38#237346100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90711378-C-A

http://identifiers.org/hco/2/GRCh38#237346418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90711851-C-A

237346418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90711851-C-T

237346429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90711862-G-A

237346479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90711924-G-T

237346530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90711975-C-T

237346621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712041-G-A

237346621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712041-G-C

237346621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712041-G-T

237346627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712047-A-G

237346643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712062-G-A

237346643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712062-G-T

http://identifiers.org/hco/2/GRCh38#237346660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90712079-C-A

237346660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712079-C-T

237346677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712095-A-G

237346921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712285-A-G

237346968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712315-T-A

237347067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712409-T-A

http://identifiers.org/hco/2/GRCh38#237347385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90712522-C-A

237347385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712522-C-G

237347416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712549-C-T

237347671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712791-G-A

http://identifiers.org/hco/2/GRCh38#237347793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90712915-C-A

237347793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712915-C-T

237347796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90712918-C-T

237347916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713038-A-G

237347959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713086-G-T

http://identifiers.org/hco/2/GRCh38#237348009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90713124-C-A

237348009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713124-C-T

237348024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713138-A-G

237348154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713256-G-A

237348229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713328-G-A

237348229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713328-G-T

237348313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713410-A-G

237348313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713410-A-T

237348609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713608-G-A

237348688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713688-T-C

237348762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713752-G-C

237348762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713752-G-T

237348771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713760-A-G

237348789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713778-A-G

237348826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90713815-C-T

237349550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714126-T-C

http://identifiers.org/hco/2/GRCh38#237350009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90714233-C-A

237350009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714233-C-T

http://identifiers.org/hco/2/GRCh38#237350034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90714258-C-A

237350078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714288-C-G

237350078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714288-C-T

237350095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714314-C-T

237350129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714339-A-G

237350136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90714349-T-C

237350186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90714399-T-C

237350186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90714399-T-G

237351032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90715541-G-A

http://identifiers.org/hco/2/GRCh38#237351280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90715775-A-C

237351280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90715775-A-G

http://identifiers.org/hco/2/GRCh38#237351316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90715788-C-A

237352589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90716003-G-A

237352614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716034-T-C

237352623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716043-G-A

237352623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716043-G-T

http://identifiers.org/hco/2/GRCh38#237353451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90716842-A-C

237353464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716855-T-G

237353498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716870-A-G

237353596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90716910-A-G

237354881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90717249-G-A

237354881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90717249-G-C

237354881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90717249-G-T

237354911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90717278-G-A

237354911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90717278-G-T

237354969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717331-G-A

237354969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717331-G-C

237354969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717331-G-T

237354970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717332-A-G

237354975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717337-G-T

237354976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717338-G-T

http://identifiers.org/hco/2/GRCh38#237355049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90717371-C-A

237355049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717371-C-G

237355049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717371-C-T

237355061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717383-A-G

http://identifiers.org/hco/2/GRCh38#237355063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90717385-C-A

237355063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717385-C-T

http://identifiers.org/hco/2/GRCh38#237355081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90717403-C-A

237355113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717424-A-G

237355113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717424-A-T

http://identifiers.org/hco/2/GRCh38#237355179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90717483-C-A

237355179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717483-C-T

237355184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717488-T-C

http://identifiers.org/hco/2/GRCh38#237355209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90717513-C-A

http://identifiers.org/hco/2/GRCh38#237355250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90717551-C-A

237355286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717587-T-G

237355387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717668-G-A

237355387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717668-G-T

237355448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717714-C-T

237355651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717880-G-A

237355651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717880-G-T

237355732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90717922-A-G

237355815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90717974-C-G

237356586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90718679-C-G

237356590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90718683-G-T

237356612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90718707-C-T

237356760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90718857-T-C

237356771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90718869-A-G

http://identifiers.org/hco/2/GRCh38#237356845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90718930-C-A

237356845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90718930-C-T

237356874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90718958-T-G

237356875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90718959-G-A

237356875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90718959-G-T

237356912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90718976-T-C

237356912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90718976-T-G

http://identifiers.org/hco/2/GRCh38#237356944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90719008-A-C

237356944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719008-A-G

http://identifiers.org/hco/2/GRCh38#237357005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90719066-C-A

237357005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719066-C-T

http://identifiers.org/hco/2/GRCh38#237357006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90719067-C-A

237357006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719067-C-T

http://identifiers.org/hco/2/GRCh38#237357016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90719080-C-A

237357016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719080-C-T

237357026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719090-G-T

237357106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719188-A-G

237357106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719188-A-T

237357288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719587-A-G

237357290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90719589-G-T

http://identifiers.org/hco/2/GRCh38#237357293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90719592-A-C

237357469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719783-G-A

237357469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719783-G-T

237357478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719790-G-A

237357478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719790-G-T

237357495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719807-G-A

237357495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719807-G-T

237357521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719832-A-G

237357528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719839-G-C

237357528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719839-G-T

237357531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719848-G-A

237357531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719848-G-C

237357531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90719848-G-T

237357693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720002-T-C

237357722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720035-A-G

http://identifiers.org/hco/2/GRCh38#237357723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90720036-C-A

237357723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720036-C-T

237357738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720051-T-C

237357740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720053-G-A

237357740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720053-G-T

http://identifiers.org/hco/2/GRCh38#237357741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90720054-C-A

237357741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720054-C-T

237357749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90720062-G-T

http://identifiers.org/hco/2/GRCh38#237357974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90720271-C-A

237357979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720276-T-G

237357980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720277-G-T

http://identifiers.org/hco/2/GRCh38#237358008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90720305-C-A

237358008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720305-C-T

237358386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720625-G-A

237358386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720625-G-T

237358389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720628-A-G

http://identifiers.org/hco/2/GRCh38#237358399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90720638-C-A

237358399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720638-C-T

237358424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720651-A-T

237358443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720670-T-C

237358447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720674-T-C

237358447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720674-T-G

http://identifiers.org/hco/2/GRCh38#237358448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90720675-C-A

237358448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720675-C-T

237358492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720704-T-C

237358614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90720828-A-G

237358755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721487-A-G

237358824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721557-C-T

237358827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721560-T-C

237358999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721690-C-T

237359018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721704-C-G

237359018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721704-C-T

237359129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90721828-T-C

http://identifiers.org/hco/2/GRCh38#237359173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90721863-A-C

237359233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90721925-A-T

237359315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722003-A-T

237359325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722013-A-G

237359330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722018-T-G

237359436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722116-G-T

237359444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722124-G-A

237359444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722124-G-T

237359528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722201-C-G

237359558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722234-G-A

237359558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722234-G-T

237359592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722271-G-C

237359614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722292-C-T

http://identifiers.org/hco/2/GRCh38#237359682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90722361-C-A

237359738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722402-C-T

237359842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722455-T-A

237359872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722485-C-G

237359872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722485-C-T

237359929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722546-C-G

237359929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722546-C-T

237359957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722573-G-C

237359957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722573-G-T

237360017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: 90722661-G-A

237360017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: 90722661-G-T

http://identifiers.org/hco/2/GRCh38#237360045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90722686-C-A

http://identifiers.org/hco/2/GRCh38#237360059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#90722700-C-A

237360059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: 90722700-C-G

237360059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: 90722700-C-T

237360198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722869-C-T

237360200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722871-T-A

237360200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722871-T-G

237360216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722887-G-A

237360216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722887-G-T

237360221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722892-G-A

237360221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722892-G-T

237360227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722898-A-T

237360285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, undefined
orthologous variants: 90722944-A-G

237360335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90722985-G-C

237360533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723153-C-T

237360919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723424-A-G

237360964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723482-C-T

http://identifiers.org/hco/2/GRCh38#237361007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90723525-C-A

http://identifiers.org/hco/2/GRCh38#237361049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90723566-C-A

237361054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723571-T-C

237361096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723612-A-G

237361157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90723673-G-A

237361211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723721-T-A

237361211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723721-T-C

237361226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723729-T-C

237361226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723729-T-G

237361267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90723766-A-G

237361676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90724144-C-T

237361722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90724185-G-C

237362014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90724423-G-T

237362083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90724483-A-G

237362300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725100-A-G

http://identifiers.org/hco/2/GRCh38#237362403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90725197-A-C

237362473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725256-G-C

http://identifiers.org/hco/2/GRCh38#237362556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90725294-A-C

237362579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725318-G-T

http://identifiers.org/hco/2/GRCh38#237362738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90725438-A-C

http://identifiers.org/hco/2/GRCh38#237362780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90725458-C-A

237362780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725458-C-T

237362853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725503-C-G

237362853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725503-C-T

http://identifiers.org/hco/2/GRCh38#237363224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90725739-C-A

237363224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90725739-C-T

237363347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90725868-C-G

237363347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90725868-C-T

237363964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727349-G-A

237364011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727387-T-C

237364029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727403-T-C

237364160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727540-G-A

237364185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727564-G-A

237364185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727564-G-T

http://identifiers.org/hco/2/GRCh38#237364298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90727667-A-C

237364298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727667-A-G

237364302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727671-C-T

237364307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727676-C-T

237364316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727685-T-G

237364329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727698-T-A

237364436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90727804-T-G

237364466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727834-A-G

237364549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727897-G-A

237364549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727897-G-T

237364638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727956-A-G

237364638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90727956-A-T

237364687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728003-A-T

237364828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728043-T-G

237364953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728078-T-C

237365137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728237-T-C

237365180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728278-T-C

237365225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728324-G-A

237365225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728324-G-C

237365232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728335-C-T

237365233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728336-G-A

237365676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90728905-T-C

237365717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90728951-G-C

237365851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90729085-C-G

237365851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90729085-C-T

237365858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90729092-G-A

237365858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90729092-G-C

237365858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90729092-G-T

237365872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90729106-T-C

237366158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729305-G-A

237366158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729305-G-T

237366167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729314-T-C

237366169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729316-T-A

237366176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729323-T-C

237366585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729731-A-G

237366671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90729801-A-G

237366769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90729896-G-A

237366862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90729989-A-G

http://identifiers.org/hco/2/GRCh38#237366919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90730046-C-A

237366934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730061-C-T

237366973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730100-G-A

237367039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730166-G-A

237367039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90730166-G-C

237367054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730181-G-A

237367102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730229-G-A

237367102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90730229-G-C

237367108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730235-C-G

237367141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90730268-C-G

237367168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730295-G-A

237367168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730295-G-T

237367183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730310-T-C

237367183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730310-T-G

http://identifiers.org/hco/2/GRCh38#237367213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90730340-C-A

237367273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90730400-T-G

http://identifiers.org/hco/2/GRCh38#237367349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90730474-C-A

237367714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730605-T-C

237367750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730641-C-T

237367932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730770-G-A

237367937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730775-G-A

237368023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730863-G-A

237368054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730894-G-A

237368135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90730956-C-T

237368208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731021-G-A

http://identifiers.org/hco/2/GRCh38#237368462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90731267-C-A

237368462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731267-C-T

237368464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731269-G-C

237368464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731269-G-T

237368495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731298-A-T

237368536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731334-T-C

http://identifiers.org/hco/2/GRCh38#237368542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90731340-C-A

237368554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731352-G-A

237368554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731352-G-T

237368735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731533-C-T

237368737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90731535-G-A

237368737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90731535-G-C

237368737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731535-G-T

237368765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731563-C-G

237368765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731563-C-T

237368833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731631-G-A

237368833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90731631-G-C

237368905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90731703-G-A

237368905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90731703-G-C

237368995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731793-G-A

237368995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90731793-G-T

237369032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90731830-G-A

http://identifiers.org/hco/2/GRCh38#237369198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90731996-A-C

237369198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90731996-A-T

237369389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732349-T-C

237369439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732402-T-C

237369487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732450-T-C

237369508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732470-A-G

237369602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732549-C-T

237369604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732551-C-T

237369686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732627-G-T

237369712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732654-C-T

237369844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90732780-T-C

237370583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90733075-T-G

http://identifiers.org/hco/2/GRCh38#237370678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90733154-C-A

237370819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90733278-T-C

237371048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90733494-G-A

237371160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90733612-T-A

237371719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90735176-G-A

237371719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90735176-G-T

237371725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 90735182-A-G

237371766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735227-C-T

237371781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735242-G-A

237371799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735260-C-G

237371799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735260-C-T

237371800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90735261-G-A

237371868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735329-C-T

237371904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90735365-C-G

237371904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735365-C-T

237371970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735431-G-A

http://identifiers.org/hco/2/GRCh38#237372006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90735467-C-A

237372006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735467-C-T

237372130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90735591-T-C

http://identifiers.org/hco/2/GRCh38#237372243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90735704-C-A

237372282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90735743-C-T

237372383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90735844-T-G

237372451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90735920-A-G

237372451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90735920-A-T

237372575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736063-C-T

237372738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736325-G-A

237372889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736491-T-A

237372963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736622-T-C

237372971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736632-C-T

237372976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736637-A-G

237373088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736770-G-C

http://identifiers.org/hco/2/GRCh38#237373200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90736886-C-A

237373200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736886-C-G

http://identifiers.org/hco/2/GRCh38#237373310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90736997-A-C

237373312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90736999-T-C

237373657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737323-T-C

237373721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737351-A-G

237373743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737377-G-A

237374171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737641-T-A

237374235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737701-G-A

237374250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737709-C-T

237374253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737712-G-A

237374283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737742-T-C

237374305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737752-T-C

237374342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90737793-T-C

http://identifiers.org/hco/2/GRCh38#237374631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90738067-C-A

http://identifiers.org/hco/2/GRCh38#237374662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90738098-C-A

237374662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90738098-C-G

237374662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90738098-C-T

237374668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90738104-G-A

http://identifiers.org/hco/2/GRCh38#237374686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90738122-C-A

237374686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90738122-C-G

237375028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90738463-G-A

237375028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 90738463-G-C

237375062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738495-G-A

237375062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738495-G-C

237376324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738520-T-C

237376517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738718-A-G

237376640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738825-A-G

237376686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738868-A-G

237376723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738905-A-G

237376731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738914-G-A

237376731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738914-G-C

237376733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738916-G-T

237376743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90738946-G-A

237376809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739018-A-G

237376809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90739018-A-T

http://identifiers.org/hco/2/GRCh38#237376875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90739084-A-C

237376890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90739099-C-G

237376938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739147-A-G

237376940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90739149-C-T

237376955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739164-G-A

237376980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739189-G-A

237376986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739195-T-C

237377025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739234-T-A

237377313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90739522-G-A

237377313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90739522-G-T

237377418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739626-C-G

http://identifiers.org/hco/2/GRCh38#237377419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90739627-C-A

237377438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739640-G-T

237377454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739655-G-T

237377461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739662-G-A

237377461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739662-G-T

237377512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739702-G-A

237377538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90739728-G-T

http://identifiers.org/hco/2/GRCh38#237377540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90739730-A-C

http://identifiers.org/hco/2/GRCh38#237377802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90740197-C-A

237377877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90740276-A-G

237377976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90740383-A-G

237378581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90740885-T-G

http://identifiers.org/hco/2/GRCh38#237378601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90740905-A-C

237378907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90741208-G-A

237378907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant
orthologous variants: 90741208-G-T

237379072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90741373-A-G

237379072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 90741373-A-T

237379268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741569-T-G

237379285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741582-T-A

237379285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741582-T-C

237379285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741582-T-G

237379307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741601-A-T

237379308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741602-C-T

237379486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741778-T-G

237379523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741813-T-A

237379535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741823-A-T

237379599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90741890-G-A

http://identifiers.org/hco/2/GRCh38#237379876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90742169-C-A

237380140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90742977-T-C

237380194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743039-G-A

237380204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743050-C-T

237380312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743153-G-T

237380326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743163-A-G

237380450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743285-G-A

237380450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743285-G-C

237380559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743373-G-A

237380813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743580-G-A

237380813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743580-G-T

http://identifiers.org/hco/2/GRCh38#237380830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90743597-C-A

237380830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743597-C-T

237380899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743657-G-C

237380899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron variant
orthologous variants: 90743657-G-T

237381021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90743779-G-A

237381021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90743779-G-T

237381149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90743907-G-A

237381149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90743907-G-T

237381219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90743977-A-G

237381219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90743977-A-T

237381230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90743988-C-T

237381237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90743995-C-G

237381237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90743995-C-T

237381278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90744036-C-G

237381278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90744036-C-T

237381291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: synonymous variant
orthologous variants: 90744049-T-C

237381295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense variant
orthologous variants: 90744053-C-T

237381306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90744064-A-G

237381356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744114-C-T

237381357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90744115-T-A

237381377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744135-G-T

http://identifiers.org/hco/2/GRCh38#237381390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90744148-C-A

237381390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744148-C-G

237381406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744164-G-A

237381410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744168-T-C

237381410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744168-T-G

237381444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90744202-C-T

237381462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90744220-C-T

237381467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90744225-G-A

237381467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90744225-G-T

237381535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744293-C-T

237381556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744314-A-G

http://identifiers.org/hco/2/GRCh38#237381580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90744333-A-C

http://identifiers.org/hco/2/GRCh38#237381629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90744367-C-A

http://identifiers.org/hco/2/GRCh38#237381633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90744371-A-C

237381813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744485-T-C

237381943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744569-G-C

237381943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744569-G-T

237381959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744585-C-G

237382034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90744669-A-G

237383171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745147-G-A

237383454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745433-T-C

http://identifiers.org/hco/2/GRCh38#237383493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90745476-A-C

237383493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745476-A-G

http://identifiers.org/hco/2/GRCh38#237383504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90745487-A-C

237383519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745504-G-A

237383519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745504-G-C

237383519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745504-G-T

237383527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745512-A-G

http://identifiers.org/hco/2/GRCh38#237383716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90745680-C-A

237383868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745774-A-G

237383895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745790-C-T

237383901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745796-G-A

237383937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90745833-T-C

http://identifiers.org/hco/2/GRCh38#237384465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90746475-A-C

237384769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90746965-C-T

http://identifiers.org/hco/2/GRCh38#237384780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90746976-C-A

237384783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90746979-C-T

237384885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747127-G-A

237384956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747210-C-T

237385069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747318-C-G

237385069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747318-C-T

237385100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747339-C-T

237385250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747462-C-T

237385497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747735-G-A

237385527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747765-G-A

237385586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90747816-C-T

http://identifiers.org/hco/2/GRCh38#237385772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90747974-C-A

237386358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748417-T-C

http://identifiers.org/hco/2/GRCh38#237386378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90748438-C-A

237386378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748438-C-G

237386378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748438-C-T

237386543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90748594-G-T

237386587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90748635-C-T

237386597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90748645-T-C

237386666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748712-T-A

237386666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748712-T-C

237386851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748873-G-A

237386865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90748884-T-G

237387215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90749157-G-A

237387428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90749358-T-C

http://identifiers.org/hco/2/GRCh38#237387435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90749365-C-A

237387435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90749365-C-T

237387573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90749515-G-A

237387573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90749515-G-T

http://identifiers.org/hco/2/GRCh38#237387607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90749549-C-A

http://identifiers.org/hco/2/GRCh38#237387887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90749829-C-A

237387887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90749829-C-G

237387887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90749829-C-T

237387970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90749912-T-C

http://identifiers.org/hco/2/GRCh38#237387996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90749938-A-C

237387996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90749938-A-T

237387997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90749939-G-A

237388033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90749975-G-A

237388033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90749975-G-C

237388033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90749975-G-T

237388317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90750273-T-A

237388582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90750519-C-G

237388582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90750519-C-T

237388873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90750808-T-C

http://identifiers.org/hco/2/GRCh38#237389264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90751169-A-C

237389264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751169-A-T

237389402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751290-G-A

237389402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751290-G-C

237389440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751316-T-C

237389461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751330-G-A

237389577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751429-G-A

http://identifiers.org/hco/2/GRCh38#237389635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90751470-C-A

237389657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751489-C-T

237389665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751497-G-T

http://identifiers.org/hco/2/GRCh38#237389717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90751552-C-A

237389720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751555-T-A

237389774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751608-C-T

237389790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751621-T-A

237389846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751673-T-C

237390091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751891-C-T

237390103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751903-C-T

237390116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751916-A-G

237390159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751959-T-C

237390186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90751982-C-T

237390389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752169-T-C

237390457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752240-T-C

237390842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752503-C-T

http://identifiers.org/hco/2/GRCh38#237390897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90752558-C-A

237391000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752661-C-T

237391017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752680-T-A

237391017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752680-T-C

237391107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90752740-C-T

237391835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90753137-C-T

237392309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90753579-C-T

237392311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90753581-C-G

237392347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90753613-C-T

237392510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90753794-T-A

http://identifiers.org/hco/2/GRCh38#237392522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90753806-C-A

237392838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90753997-G-A

237393023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754142-C-T

237393174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754269-T-G

237393218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754313-T-A

237393688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754700-G-A

237393797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754805-T-C

237393840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754846-C-G

237393840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754846-C-T

237393848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754854-C-T

237393863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90754872-C-T

http://identifiers.org/hco/2/GRCh38#237394287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90755318-C-A

237394400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90755410-G-T

237394857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90755852-C-G

237394857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90755852-C-T

237394976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90755971-G-A

237395001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90755996-T-C

237395238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756233-C-G

237395243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756235-T-C

237395275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756266-C-G

237395275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756266-C-T

http://identifiers.org/hco/2/GRCh38#237395314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90756306-C-A

http://identifiers.org/hco/2/GRCh38#237395347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90756340-C-A

237395432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756421-G-A

237395432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756421-G-C

237395480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756468-T-G

237395485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756473-G-A

237395516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756500-G-A

http://identifiers.org/hco/2/GRCh38#237395529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90756514-C-A

237395698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756683-G-C

237395785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756761-T-A

237395785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756761-T-C

237395823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90756796-C-T

237395938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90756913-C-T

http://identifiers.org/hco/2/GRCh38#237395994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90756967-C-A

237395994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90756967-C-T

237396455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90757407-T-C

http://identifiers.org/hco/2/GRCh38#237396691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90757839-C-A

237396691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90757839-C-G

237396691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90757839-C-T

237396748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90757883-G-A

237396769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90757904-G-C

237396856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90757989-G-A

http://identifiers.org/hco/2/GRCh38#237396861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90757994-C-A

237396861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90757994-C-T

237396930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90758049-G-A

237396930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90758049-G-T

237396949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90758067-G-A

237397008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90758133-T-A

237397008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90758133-T-G

237397880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90758945-C-T

237398071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90759076-G-A

http://identifiers.org/hco/2/GRCh38#237398150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90759137-A-C

237398276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90759252-G-A

237398276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90759252-G-T

237398558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90759500-T-G

237399863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90759553-T-C

237399916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90759606-C-T

237400347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760118-A-G

http://identifiers.org/hco/2/GRCh38#237400404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90760172-C-A

237400404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760172-C-T

237400453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760230-G-T

237400458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760235-G-A

237402584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760310-G-A

http://identifiers.org/hco/2/GRCh38#237402628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90760354-A-C

237402672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760392-G-A

237402725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760441-T-A

237402857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760565-A-G

237403093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760769-G-A

237403279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90760917-G-A

237403313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90760933-A-G

http://identifiers.org/hco/2/GRCh38#237403495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90761089-A-C

237403768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761330-C-T

237403770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761332-C-G

237403770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761332-C-T

237403837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761392-C-T

237403981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761630-C-G

237404003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761720-G-A

237404003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761720-G-T

237404255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761931-G-A

237404255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761931-G-C

237404298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761973-G-A

237404298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90761973-G-C

237405042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763012-C-G

237405042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763012-C-T

237405220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763160-A-G

237405403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763334-T-C

237405646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90763606-G-A

237406478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764377-G-A

237406480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764379-G-A

237406480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764379-G-T

237406522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764412-C-T

237406555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764446-G-C

237406585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764476-G-A

237406585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764476-G-T

237406881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90764977-G-T

237407043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765136-A-G

237407070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765150-T-G

237407312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765452-A-G

237407315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765455-C-T

237407329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765478-C-G

237407364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765499-C-T

237407809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90765993-T-C

237407926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766108-T-A

237408145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766314-T-C

237408308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766409-C-T

237408479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766542-G-A

237408684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766745-T-C

237408684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766745-T-G

237408717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90766778-T-G

237409562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767575-G-T

237409691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767694-C-T

237409759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767750-G-A

237409799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90767800-C-T

237410279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768228-T-C

237410336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90768265-T-G

237410951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90768726-C-T

http://identifiers.org/hco/2/GRCh38#237411657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90769373-C-A

237411675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90769392-T-C

237411848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90769506-A-G

237411851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90769509-A-T

237411878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90769530-G-A

http://identifiers.org/hco/2/GRCh38#237412219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90769873-C-A

237412691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770347-C-T

237412727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770368-G-A

237412787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770410-C-G

237412822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770446-T-C

237412902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770501-G-A

237413225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770806-C-G

237413225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90770806-C-T

237413420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771001-T-A

237413499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771058-A-G

237413637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771176-T-C

237413658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771195-C-T

237413744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771289-A-G

237413802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771344-G-A

http://identifiers.org/hco/2/GRCh38#237413845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#90771377-C-A

237413848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771380-C-T

237413850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771382-T-C

237413939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90771454-G-T

237413973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90771487-G-A

237413973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90771487-G-C

237413973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90771487-G-T

237414182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90771699-G-T

237414193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90771710-T-C