204131073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133308042-G-A

204131073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133308042-G-T

http://identifiers.org/hco/1/GRCh38#204131128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307994-C-A

204131128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133307994-C-T

204131151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133307973-G-T

http://identifiers.org/hco/1/GRCh38#204131233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307915-C-A

204131233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133307915-C-T

http://identifiers.org/hco/1/GRCh38#204131254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307896-C-A

http://identifiers.org/hco/1/GRCh38#204131291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307866-C-A

204131291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133307866-C-T

204131536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133307709-C-T

http://identifiers.org/hco/1/GRCh38#204131547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307698-C-A

204131580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133307675-G-A

204131580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133307675-G-T

204131745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133307526-A-G

204131766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133307498-A-G

http://identifiers.org/hco/1/GRCh38#204131859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307416-C-A

204131859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133307416-C-T

204131867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133307408-C-T

204131869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133307406-G-A

204131869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133307406-G-T

http://identifiers.org/hco/1/GRCh38#204131899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307378-C-A

204131973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3 prime UTR variant
orthologous variants: 133307294-G-A

204131973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3 prime UTR variant
orthologous variants: 133307294-G-C

204131973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3 prime UTR variant
orthologous variants: 133307294-G-T

204131978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3 prime UTR variant
orthologous variants: 133307289-G-A

http://identifiers.org/hco/1/GRCh38#204132110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133307194-C-A

204132203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 133307106-G-A

204132203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 133307106-G-T

http://identifiers.org/hco/1/GRCh38#204132382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133306961-C-A

204132425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133306936-T-A

204132594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133306688-G-C

204132717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133306582-G-A

204134658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133306122-G-A

204134762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133306044-A-G

http://identifiers.org/hco/1/GRCh38#204134782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133306024-C-A

204134784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133306022-G-A

204134784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133306022-G-T

204134802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133306004-G-A

204134802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133306004-G-C

204134802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133306004-G-T

204135500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133305884-C-T

204135579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133305816-C-G

204135952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133305502-T-C

204137032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304812-G-C

204137038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304806-G-A

204137039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304805-T-G

204137107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133304784-G-A

204137107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133304784-G-C

204137204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133304687-T-C

204137204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133304687-T-G

http://identifiers.org/hco/1/GRCh38#204137213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, incomplete_terminal_codon_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133304678-C-A

204137213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, incomplete_terminal_codon_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133304678-C-G

204137213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, incomplete_terminal_codon_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133304678-C-T

204137238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133304653-C-T

204137313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304588-T-C

204137383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304544-G-A

204137383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304544-G-T

204137444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304500-G-A

204137503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304448-G-C

204137996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133304151-G-A

204138555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133303804-T-C

http://identifiers.org/hco/1/GRCh38#204138758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133303586-C-A

http://identifiers.org/hco/1/GRCh38#204138779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133303568-C-A

204138779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133303568-C-T

204138791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133303558-G-T

204139029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133303251-G-C

204139035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133303245-T-C

204139211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133303082-C-T

204139788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302632-T-C

204139996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302389-C-T

204140006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302375-G-C

204140006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302375-G-T

204140067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133302314-A-G

204140132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302249-G-A

204140167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302216-A-G

204140209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133302176-A-G

http://identifiers.org/hco/1/GRCh38#204140243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133302164-C-A

204141130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133301196-G-A

204141130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133301196-G-T

http://identifiers.org/hco/1/GRCh38#204141184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133301144-A-C

204141184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133301144-A-G

http://identifiers.org/hco/1/GRCh38#204141463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133300865-C-A

204141463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133300865-C-T

http://identifiers.org/hco/1/GRCh38#204141551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133300794-C-A

204141551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300794-C-G

204141551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300794-C-T

204141695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300662-T-C

http://identifiers.org/hco/1/GRCh38#204141867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133300493-A-C

204141925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300438-G-A

204141925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300438-G-C

204141925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300438-G-T

http://identifiers.org/hco/1/GRCh38#204141973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133300413-C-A

204141973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300413-C-T

204142028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300372-T-C

http://identifiers.org/hco/1/GRCh38#204142059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133300345-C-A

204142060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300344-A-G

204142180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300271-A-G

204142217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133300216-T-G

204142275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133300164-G-T

204142278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133300161-C-T

http://identifiers.org/hco/1/GRCh38#204142279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133300160-C-A

204142405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133300060-T-A

204142437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133300049-G-C

204142783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133299820-C-T

204143189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133299555-T-C

204143281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133299477-T-G

204143480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133299287-C-T

204143670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133299162-C-T

204143766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133299065-G-A

204143766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133299065-G-T

204143818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133299012-A-G

204143822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133299008-C-G

204143951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133298922-A-T

204144617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133298435-C-T

204144852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133298238-C-G

204144992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133298093-T-C

204145180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133297987-G-A

204145461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133297810-T-C

204145744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133297591-C-T

204145822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133297476-C-T

204146225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133297002-C-T

http://identifiers.org/hco/1/GRCh38#204146509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133296731-C-A

204146509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133296731-C-T

204146511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133296730-G-A

204146511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133296730-G-T

204146549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133296698-C-T

204146571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133296676-G-T

204146593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133296654-G-A

204146786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133296465-G-A

204146876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133296379-G-C

204146883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133296372-G-C

204146883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133296372-G-T

204146896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133296359-G-A

204146896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133296359-G-T

204146952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133296306-G-A

204146952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133296306-G-T

204147121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133296141-G-A

204147121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133296141-G-T

204147226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133296034-G-A

204147229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133296031-G-A

204147326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133295948-C-T

204147488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, missense_variant
orthologous variants: 133295798-A-T

204147505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 133295772-C-T

http://identifiers.org/hco/1/GRCh38#204147558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133295713-C-A

204147558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 133295713-C-T

204147726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133295546-G-C

204147767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133295509-T-C

http://identifiers.org/hco/1/GRCh38#204147842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133295459-C-A

204147842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133295459-C-T

204147946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133295369-T-G

204148378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133294946-G-A

204148378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133294946-G-T

204148519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133294816-G-A

204148947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133294443-C-T

204148991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133294390-C-T

204149232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133294113-T-C

204149259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293998-C-T

204149369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293858-T-A

204149555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293702-A-G

http://identifiers.org/hco/1/GRCh38#204149572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293685-C-A

204149572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293685-C-T

http://identifiers.org/hco/1/GRCh38#204149719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293555-C-A

204149719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, missense_variant
orthologous variants: 133293555-C-T

http://identifiers.org/hco/1/GRCh38#204149771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293503-C-A

204149771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133293503-C-T

http://identifiers.org/hco/1/GRCh38#204149817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293457-C-A

204149817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron_variant, missense_variant
orthologous variants: 133293457-C-T

http://identifiers.org/hco/1/GRCh38#204149949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293325-C-A

204150013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293263-T-C

204150013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293263-T-G

http://identifiers.org/hco/1/GRCh38#204150081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293200-C-A

204150081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293200-C-G

http://identifiers.org/hco/1/GRCh38#204150082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133293199-C-A

204150154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293150-T-C

204150224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133293078-G-A

http://identifiers.org/hco/1/GRCh38#204150356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133292946-A-C

204150369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292938-G-A

204150369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292938-G-C

204150369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292938-G-T

204150412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292894-T-C

204150412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292894-T-G

204150585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292701-G-A

204150585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292701-G-T

204150600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292686-A-G

204150619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292667-G-T

204150623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292663-T-A

204150623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292663-T-C

204150643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292646-G-A

204150643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292646-G-T

http://identifiers.org/hco/1/GRCh38#204150882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133292454-C-A

204150882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292454-C-T

204150962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292374-G-A

204150962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133292374-G-T

204151015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292329-T-A

204151015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292329-T-C

204151015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292329-T-G

204151017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292327-T-C

http://identifiers.org/hco/1/GRCh38#204151028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133292316-C-A

204151028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292316-C-G

204151028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292316-C-T

204151039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292304-G-A

204151039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292304-G-T

204151047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292300-T-A

204151047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292300-T-G

204151050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292297-G-A

204151082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292252-G-A

204151141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292183-A-G

204151141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292183-A-T

http://identifiers.org/hco/1/GRCh38#204151146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133292178-C-A

204151146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292178-C-T

204151162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292162-C-G

204151208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292136-G-C

204151267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292080-G-A

204151267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292080-G-C

204151267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292080-G-T

204151291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292057-G-A

204151291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292057-G-T

http://identifiers.org/hco/1/GRCh38#204151327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133292023-C-A

http://identifiers.org/hco/1/GRCh38#204151334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133292016-C-A

204151334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133292016-C-T

204151382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133291980-G-A

204151382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133291980-G-C

204151382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133291980-G-T

http://identifiers.org/hco/1/GRCh38#204151407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133291957-A-C

204151407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133291957-A-G

204151407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133291957-A-T

204151516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133291833-G-A

204151516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133291833-G-T

204151565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: intron variant
orthologous variants: 133291784-C-G

204151674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133291675-G-A

204151674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133291675-G-C

204151674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133291675-G-T

204151688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 133291661-G-C

204151688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 133291661-G-T

204151749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133291603-G-A

204151749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133291603-G-C

204151749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 133291603-G-T

204151838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 133291514-A-G

204151838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 133291514-A-T

204151899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291451-G-A

204151899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291451-G-T

204151902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291448-G-A

204151902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291448-G-C

204151902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291448-G-T

204151906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291444-G-A

204151906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291444-G-C

204151906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291444-G-T

http://identifiers.org/hco/1/GRCh38#204152015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133291335-C-A

204152015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291335-C-T

http://identifiers.org/hco/1/GRCh38#204152018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133291332-C-A

http://identifiers.org/hco/1/GRCh38#204152032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#133291318-C-A

204152032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25575
most severe consequence: 5 prime UTR variant
orthologous variants: 133291318-C-T